Entity Name	Entity type	Gene Symbol	Sources(; separated)	Level4	Level3	Level2	Model_Of_Inheritance	Phenotypes	Omim	Orphanet	HPO	Publications	Description	Flagged	GEL_Status	UserRatings_Green_amber_red	version	ready	Mode of pathogenicity	EnsemblId(GRch37)	EnsemblId(GRch38)	HGNC	Position Chromosome	Position GRCh37 Start	Position GRCh37 End	Position GRCh38 Start	Position GRCh38 End	STR Repeated Sequence	STR Normal Repeats	STR Pathogenic Repeats	Region Haploinsufficiency Score	Region Triplosensitivity Score	Region Required Overlap Percentage	Region Variant Type	Region Verbose Name
AAAS	gene	AAAS	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Achalasia-addisonianism-alacrimia syndrome, 231550 (3)						False	3	0;0;0	0.109	False		ENSG00000094914	ENSG00000094914	HGNC:13666													
AARS2	gene	AARS2	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Combined oxidative phosphorylation deficiency 8, 614096 (3)						False	3	0;0;0	0.109	False		ENSG00000124608	ENSG00000124608	HGNC:21022													
ABAT	gene	ABAT	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	GABA-transaminase deficiency, 613163 (3)						False	3	0;0;0	0.109	False		ENSG00000183044	ENSG00000183044	HGNC:23													
ABCA12	gene	ABCA12	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Ichthyosis, congenital, autosomal recessive 4A, 601277 (3)						False	3	0;0;0	0.109	False		ENSG00000144452	ENSG00000144452	HGNC:14637													
ABCA3	gene	ABCA3	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Surfactant metabolism dysfunction, pulmonary, 3, 610921 (3)						False	3	0;0;0	0.109	False		ENSG00000167972	ENSG00000167972	HGNC:33													
ABCB11	gene	ABCB11	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Cholestasis, progressive familial intrahepatic 2, 601847 (3)						False	3	0;0;0	0.109	False		ENSG00000073734	ENSG00000073734	HGNC:42													
ABCB4	gene	ABCB4	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Cholestasis, progressive familial intrahepatic 3, 602347 (3)						False	3	0;0;0	0.109	False		ENSG00000005471	ENSG00000005471	HGNC:45													
ABCB7	gene	ABCB7	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	X-LINKED: hemizygous mutation in males, biallelic mutations in females	Anemia, sideroblastic, with ataxia, 301310 (3)						False	3	0;0;0	0.109	False		ENSG00000131269	ENSG00000131269	HGNC:48													
ABCC8	gene	ABCC8	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Hyperinsulinemic hypoglycemia, familial, 1, 256450 (3)						False	3	0;0;0	0.109	False		ENSG00000006071	ENSG00000006071	HGNC:59													
ABCD1	gene	ABCD1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	X-LINKED: hemizygous mutation in males, biallelic mutations in females	Adrenoleukodystrophy, 300100 (3)						False	3	0;0;0	0.109	False		ENSG00000101986	ENSG00000101986	HGNC:61													
ABHD5	gene	ABHD5	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Chanarin-Dorfman syndrome, 275630 (3)						False	3	0;0;0	0.109	False		ENSG00000011198	ENSG00000011198	HGNC:21396													
ACAD9	gene	ACAD9	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Mitochondrial complex I deficiency due to ACAD9 deficiency, 611126 (3)						False	3	0;0;0	0.109	False		ENSG00000177646	ENSG00000177646	HGNC:21497													
ACADM	gene	ACADM	Expert Review;Expert Review Green	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Acyl-CoA dehydrogenase, medium chain, deficiency of, MIM #201450						False	3	100;0;0	0.109	True		ENSG00000117054	ENSG00000117054	HGNC:89													
ACADVL	gene	ACADVL	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	VLCAD deficiency, 201475 (3)						False	3	0;0;0	0.109	False		ENSG00000072778	ENSG00000072778	HGNC:92													
ACAT1	gene	ACAT1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Alpha-methylacetoacetic aciduria, 203750 (3)						False	3	0;0;0	0.109	False		ENSG00000075239	ENSG00000075239	HGNC:93													
ACE	gene	ACE	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Renal tubular dysgenesis, 267430 (3)						False	3	0;0;0	0.109	False		ENSG00000159640	ENSG00000159640	HGNC:2707													
ACO2	gene	ACO2	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Infantile cerebellar-retinal degeneration, 614559 (3)						False	3	0;0;0	0.109	False		ENSG00000100412	ENSG00000100412	HGNC:118													
ACOX1	gene	ACOX1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Peroxisomal acyl-CoA oxidase deficiency, 264470 (3)						False	3	0;0;0	0.109	False		ENSG00000161533	ENSG00000161533	HGNC:119													
ACTA1	gene	ACTA1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Myopathy, congenital, with fiber-type disproportion 1, 255310 (3)						False	3	0;0;0	0.109	False		ENSG00000143632	ENSG00000143632	HGNC:129													
ADA	gene	ADA	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Adenosine deaminase deficiency, partial, 102700 (3)						False	3	0;0;0	0.109	False		ENSG00000196839	ENSG00000196839	HGNC:186													
ADA2	gene	ADA2	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Polyarteritis nodosa, childhood-onset, 615688 (3)						False	3	0;0;0	0.109	False		ENSG00000093072	ENSG00000093072	HGNC:1839													
ADAMTS13	gene	ADAMTS13	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Thrombotic thrombocytopenic purpura, familial, 274150 (3)						False	3	0;0;0	0.109	False		ENSG00000160323	ENSG00000160323	HGNC:1366													
ADAMTS2	gene	ADAMTS2	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Ehlers-Danlos syndrome, type VIIC, 225410 (3)						False	3	0;0;0	0.109	False		ENSG00000087116	ENSG00000087116	HGNC:218													
ADAMTSL2	gene	ADAMTSL2	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Geleophysic dysplasia 1, 231050 (3)						False	3	0;0;0	0.109	False		ENSG00000197859	ENSG00000197859	HGNC:14631													
ADAR	gene	ADAR	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Aicardi-Goutieres syndrome 6, 615010 (3)						False	3	0;0;0	0.109	False		ENSG00000160710	ENSG00000160710	HGNC:225													
ADAT3	gene	ADAT3	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Mental retardation, autosomal recessive 36, 615286 (3)						False	3	0;0;0	0.109	False		ENSG00000213638	ENSG00000213638	HGNC:25151													
ADGRG1	gene	ADGRG1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Polymicrogyria, bilateral frontoparietal, 606854 (3)						False	3	0;0;0	0.109	False		ENSG00000205336	ENSG00000205336	HGNC:4512													
ADGRV1	gene	ADGRV1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Usher syndrome, type 2C, 605472 (3)						False	3	0;0;0	0.109	False		ENSG00000164199	ENSG00000164199	HGNC:17416													
ADSL	gene	ADSL	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Adenylosuccinase deficiency, 103050 (3)						False	3	0;0;0	0.109	False		ENSG00000239900	ENSG00000239900	HGNC:291													
AGA	gene	AGA	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Aspartylglucosaminuria, 208400 (3)						False	3	0;0;0	0.109	False		ENSG00000038002	ENSG00000038002	HGNC:318													
AGBL5	gene	AGBL5	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Retinitis pigmentosa 75, 617023 (3), Autosomal recessive						False	3	0;0;0	0.109	False		ENSG00000084693	ENSG00000084693	HGNC:26147													
AGK	gene	AGK	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Sengers syndrome, 212350 (3)						False	3	0;0;0	0.109	False		ENSG00000006530	ENSG00000006530	HGNC:21869													
AGL	gene	AGL	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Glycogen storage disease IIIa, 232400 (3)						False	3	0;0;0	0.109	False		ENSG00000162688	ENSG00000162688	HGNC:321													
AGPS	gene	AGPS	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Chondrodysplasia punctata, rhizomelic, type 3, 600121 (3)						False	3	0;0;0	0.109	False		ENSG00000018510	ENSG00000018510	HGNC:327													
AGRN	gene	AGRN	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Myasthenic syndrome, congenital, 8, with pre- and postsynaptic defects, 615120 (3)						False	3	0;0;0	0.109	False		ENSG00000188157	ENSG00000188157	HGNC:329													
AGT	gene	AGT	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Renal tubular dysgenesis, 267430 (3)						False	3	0;0;0	0.109	False		ENSG00000135744	ENSG00000135744	HGNC:333													
AGXT	gene	AGXT	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Hyperoxaluria, primary, type 1, 259900 (3)						False	3	0;0;0	0.109	False		ENSG00000172482	ENSG00000172482	HGNC:341													
AHI1	gene	AHI1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Joubert syndrome-3, 608629 (3)						False	3	0;0;0	0.109	False		ENSG00000135541	ENSG00000135541	HGNC:21575													
AIFM1	gene	AIFM1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	X-LINKED: hemizygous mutation in males, biallelic mutations in females	Cowchock syndrome, 310490 (3)						False	3	0;0;0	0.109	False		ENSG00000156709	ENSG00000156709	HGNC:8768													
AIMP1	gene	AIMP1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Leukodystrophy, hypomyelinating, 3, 260600 (3)						False	3	0;0;0	0.109	False		ENSG00000164022	ENSG00000164022	HGNC:10648													
AIPL1	gene	AIPL1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Cone-rod dystrophy, 604393 (3)						False	3	0;0;0	0.109	False		ENSG00000129221	ENSG00000129221	HGNC:359													
AK2	gene	AK2	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Reticular dysgenesis, 267500 (3)						False	3	0;0;0	0.109	False		ENSG00000004455	ENSG00000004455	HGNC:362													
AKR1D1	gene	AKR1D1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Bile acid synthesis defect, congenital, 2, 235555 (3)						False	3	0;0;0	0.109	False		ENSG00000122787	ENSG00000122787	HGNC:388													
ALAD	gene	ALAD	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Porphyria, acute hepatic, 612740 (3)						False	3	0;0;0	0.109	False		ENSG00000148218	ENSG00000148218	HGNC:395													
ALDH18A1	gene	ALDH18A1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Spastic paraplegia 9B, autosomal recessive, 616586 (3)						False	3	0;0;0	0.109	False		ENSG00000059573	ENSG00000059573	HGNC:9722													
ALDH1A3	gene	ALDH1A3	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Microphthalmia, isolated 8, 615113 (3)						False	3	0;0;0	0.109	False		ENSG00000184254	ENSG00000184254	HGNC:409													
ALDH3A2	gene	ALDH3A2	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Sjogren-Larsson syndrome, 270200 (3)						False	3	0;0;0	0.109	False		ENSG00000072210	ENSG00000072210	HGNC:403													
ALDH5A1	gene	ALDH5A1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Succinic semialdehyde dehydrogenase deficiency, 271980 (3)						False	3	0;0;0	0.109	False		ENSG00000112294	ENSG00000112294	HGNC:408													
ALDH7A1	gene	ALDH7A1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Epilepsy, pyridoxine-dependent, 266100 (3)						False	3	0;0;0	0.109	False		ENSG00000164904	ENSG00000164904	HGNC:877													
ALDOB	gene	ALDOB	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Fructose intolerance, 229600 (3)						False	3	0;0;0	0.109	False		ENSG00000136872	ENSG00000136872	HGNC:417													
ALG1	gene	ALG1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Congenital disorder of glycosylation, type Ik, 608540 (3)						False	3	0;0;0	0.109	False		ENSG00000033011	ENSG00000033011	HGNC:18294													
ALG11	gene	ALG11	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Congenital disorder of glycosylation, type Ip, 613661 (3)						False	3	0;0;0	0.109	False		ENSG00000253710	ENSG00000253710	HGNC:32456													
ALG12	gene	ALG12	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Congenital disorder of glycosylation, type Ig, 607143 (3)						False	3	0;0;0	0.109	False		ENSG00000182858	ENSG00000182858	HGNC:19358													
ALG2	gene	ALG2	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Myasthenic syndrome, congenital, 14, with tubular aggregates, 616228 (3)						False	3	0;100;0	0.109	False		ENSG00000119523	ENSG00000119523	HGNC:23159													
ALG3	gene	ALG3	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Congenital disorder of glycosylation, type Id, 601110 (3)						False	3	0;0;0	0.109	False		ENSG00000214160	ENSG00000214160	HGNC:23056													
ALG6	gene	ALG6	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Congenital disorder of glycosylation, type Ic, 603147 (3)						False	3	0;0;0	0.109	False		ENSG00000088035	ENSG00000088035	HGNC:23157													
ALG8	gene	ALG8	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Congenital disorder of glycosylation, type Ih, 608104 (3)						False	3	0;0;0	0.109	False		ENSG00000159063	ENSG00000159063	HGNC:23161													
ALG9	gene	ALG9	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Congenital disorder of glycosylation, type Il, 608776 (3)						False	3	0;0;0	0.109	False		ENSG00000086848	ENSG00000086848	HGNC:15672													
ALMS1	gene	ALMS1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Alstrom syndrome, 203800 (3)						False	3	0;0;0	0.109	False		ENSG00000116127	ENSG00000116127	HGNC:428													
ALOX12B	gene	ALOX12B	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Ichthyosis, congenital, autosomal recessive 2, 242100 (3)						False	3	0;0;0	0.109	False		ENSG00000179477	ENSG00000179477	HGNC:430													
ALOXE3	gene	ALOXE3	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Ichthyosis, congenital, autosomal recessive 3, 606545 (3)						False	3	0;0;0	0.109	False		ENSG00000179148	ENSG00000179148	HGNC:13743													
ALPL	gene	ALPL	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Hypophosphatasia, infantile, 241500 (3)						False	3	0;0;0	0.109	False		ENSG00000162551	ENSG00000162551	HGNC:438													
ALS2	gene	ALS2	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Primary lateral sclerosis, juvenile, 606353 (3)						False	3	0;0;0	0.109	False		ENSG00000003393	ENSG00000003393	HGNC:443													
AMPD2	gene	AMPD2	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Pontocerebellar hypoplasia, type 9, 615809 (3)						False	3	0;0;0	0.109	False		ENSG00000116337	ENSG00000116337	HGNC:469													
AMT	gene	AMT	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Glycine encephalopathy, 605899 (3)						False	3	0;0;0	0.109	False		ENSG00000145020	ENSG00000145020	HGNC:473													
ANKS6	gene	ANKS6	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Nephronophthisis 16, 615382 (3)						False	3	0;0;0	0.109	False		ENSG00000165138	ENSG00000165138	HGNC:26724													
ANTXR1	gene	ANTXR1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	GAPO syndrome, 230740 (3)						False	3	0;0;0	0.109	False		ENSG00000169604	ENSG00000169604	HGNC:21014													
ANTXR2	gene	ANTXR2	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Hyaline fibromatosis syndrome, 228600 (3)						False	3	0;0;0	0.109	False		ENSG00000163297	ENSG00000163297	HGNC:21732													
AP1S2	gene	AP1S2	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	X-LINKED: hemizygous mutation in males, biallelic mutations in females	Mental retardation, X-linked syndromic 5, 304340 (3)						False	3	0;0;0	0.109	False		ENSG00000182287	ENSG00000182287	HGNC:560													
AP3B2	gene	AP3B2	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Epileptic encephalopathy, early infantile, 48, 617276 (3), Autosomal recessive						False	3	0;0;0	0.109	False		ENSG00000103723	ENSG00000103723	HGNC:567													
AP4B1	gene	AP4B1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Spastic paraplegia 47, autosomal recessive, 614066 (3)						False	3	0;0;0	0.109	False		ENSG00000134262	ENSG00000134262	HGNC:572													
AP4M1	gene	AP4M1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Spastic paraplegia 50, autosomal recessive, 612936 (3)						False	3	0;0;0	0.109	False		ENSG00000221838	ENSG00000221838	HGNC:574													
AP4S1	gene	AP4S1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Spastic paraplegia 52, autosomal recessive, 614067 (3)						False	3	0;0;0	0.109	False		ENSG00000100478	ENSG00000100478	HGNC:575													
APOPT1	gene	APOPT1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Mitochondrial complex IV deficiency, 220110 (3)						False	3	0;0;0	0.109	False		ENSG00000256053	ENSG00000256053	HGNC:20492													
APTX	gene	APTX	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Ataxia, early-onset, with oculomotor apraxia and hypoalbuminemia, 208920 (3)						False	3	0;0;0	0.109	False		ENSG00000137074	ENSG00000137074	HGNC:15984													
AQP2	gene	AQP2	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Diabetes insipidus, nephrogenic, 125800 (3)						False	3	0;0;0	0.109	False		ENSG00000167580	ENSG00000167580	HGNC:634													
ARFGEF2	gene	ARFGEF2	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Periventricular heterotopia with microcephaly, 608097 (3)						False	3	0;0;0	0.109	False		ENSG00000124198	ENSG00000124198	HGNC:15853													
ARG1	gene	ARG1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Argininemia, 207800 (3)						False	3	0;0;0	0.109	False		ENSG00000118520	ENSG00000118520	HGNC:663													
ARHGEF9	gene	ARHGEF9	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	X-LINKED: hemizygous mutation in males, biallelic mutations in females	Epileptic encephalopathy, early infantile, 8, 300607 (3)						False	3	0;0;0	0.109	False		ENSG00000131089	ENSG00000131089	HGNC:14561													
ARL13B	gene	ARL13B	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Joubert syndrome 8, 612291 (3)						False	3	0;0;0	0.109	False		ENSG00000169379	ENSG00000169379	HGNC:25419													
ARL6	gene	ARL6	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Bardet-Biedl syndrome 3, 600151 (3)						False	3	0;0;0	0.109	False		ENSG00000113966	ENSG00000113966	HGNC:13210													
ARMC4	gene	ARMC4	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Ciliary dyskinesia, primary, 23, 615451 (3)						False	3	0;0;0	0.109	False		ENSG00000169126	ENSG00000169126	HGNC:25583													
ARPC1B	gene	ARPC1B	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Platelet abnormalities with eosinophilia and immune-mediated inflammatory disease, 617718 (3), Autosomal recessive						False	3	0;0;0	0.109	False		ENSG00000130429	ENSG00000130429	HGNC:704													
ARSA	gene	ARSA	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Metachromatic leukodystrophy, 250100 (3)						False	3	0;0;0	0.109	False		ENSG00000100299	ENSG00000100299	HGNC:713													
ARSB	gene	ARSB	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Mucopolysaccharidosis type VI (Maroteaux-Lamy), 253200 (3)						False	3	0;0;0	0.109	False		ENSG00000113273	ENSG00000113273	HGNC:714													
ARV1	gene	ARV1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Epileptic encephalopathy, early infantile, 38, 617020 (3), Autosomal recessive						False	3	0;0;0	0.109	False		ENSG00000173409	ENSG00000173409	HGNC:29561													
ARX	gene	ARX	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	X-LINKED: hemizygous mutation in males, biallelic mutations in females	Hydranencephaly with abnormal genitalia, 300215 (3)						False	3	0;0;0	0.109	False		ENSG00000004848	ENSG00000004848	HGNC:18060													
ASAH1	gene	ASAH1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Farber lipogranulomatosis, 228000 (3)						False	3	0;0;0	0.109	False		ENSG00000104763	ENSG00000104763	HGNC:735													
ASCC1	gene	ASCC1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Spinal muscular atrophy with congenital bone fractures 2, MIM#616867						False	3	0;0;0	0.109	True		ENSG00000138303	ENSG00000138303	HGNC:24268													
ASL	gene	ASL	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Argininosuccinic aciduria, 207900 (3)						False	3	0;0;0	0.109	False		ENSG00000126522	ENSG00000126522	HGNC:746													
ASNS	gene	ASNS	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Asparagine synthetase deficiency, 615574 (3)						False	3	0;0;0	0.109	False		ENSG00000070669	ENSG00000070669	HGNC:753													
ASPA	gene	ASPA	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Canavan disease, 271900 (3)						False	3	0;0;0	0.109	False		ENSG00000108381	ENSG00000108381	HGNC:756													
ASPM	gene	ASPM	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Microcephaly 5, primary, autosomal recessive, 608716 (3)						False	3	0;0;0	0.109	False		ENSG00000066279	ENSG00000066279	HGNC:19048													
ASS1	gene	ASS1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Citrullinemia, 215700 (3)						False	3	0;0;0	0.109	False		ENSG00000130707	ENSG00000130707	HGNC:758													
ATAD1	gene	ATAD1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Hyperekplexia 4, 618011 (3), Autosomal recessive						False	3	0;0;0	0.109	False		ENSG00000138138	ENSG00000138138	HGNC:25903													
ATCAY	gene	ATCAY	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Ataxia, cerebellar, Cayman type, 601238 (3)						False	3	0;0;0	0.109	False		ENSG00000167654	ENSG00000167654	HGNC:779													
ATF6	gene	ATF6	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Achromatopsia 7, 616517 (3), Autosomal recessive						False	3	0;0;0	0.109	False		ENSG00000118217	ENSG00000118217	HGNC:791													
ATM	gene	ATM	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Ataxia-telangiectasia, 208900 (3)						False	3	0;0;0	0.109	False		ENSG00000149311	ENSG00000149311	HGNC:795													
ATOH7	gene	ATOH7	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Persistent hyperplastic primary vitreous, autosomal recessive, 221900 (3)						False	3	0;0;0	0.109	False		ENSG00000179774	ENSG00000179774	HGNC:13907													
ATP13A2	gene	ATP13A2	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Spastic paraplegia 78, autosomal recessive, 617225 (3)						False	3	0;0;0	0.109	False		ENSG00000159363	ENSG00000159363	HGNC:30213													
ATP6AP1	gene	ATP6AP1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	X-LINKED: hemizygous mutation in males, biallelic mutations in females	Immunodeficiency 47, 300972 (3), X-linked recessive						False	3	0;0;0	0.109	False		ENSG00000071553	ENSG00000071553	HGNC:868													
ATP6V0A2	gene	ATP6V0A2	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Cutis laxa, autosomal recessive, type IIA, 219200 (3)						False	3	0;0;0	0.109	False		ENSG00000185344	ENSG00000185344	HGNC:18481													
ATP6V0A4	gene	ATP6V0A4	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Renal tubular acidosis, distal, autosomal recessive, 602722 (3)						False	3	0;0;0	0.109	False		ENSG00000105929	ENSG00000105929	HGNC:866													
ATP6V1B1	gene	ATP6V1B1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Renal tubular acidosis with deafness, 267300 (3)						False	3	0;0;0	0.109	False		ENSG00000116039	ENSG00000116039	HGNC:853													
ATP7A	gene	ATP7A	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	X-LINKED: hemizygous mutation in males, biallelic mutations in females	Menkes disease, 309400 (3)						False	3	0;0;0	0.109	False		ENSG00000165240	ENSG00000165240	HGNC:869													
ATP7B	gene	ATP7B	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Wilson disease, 277900 (3)						False	3	0;0;0	0.109	False		ENSG00000123191	ENSG00000123191	HGNC:870													
ATP8A2	gene	ATP8A2	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	?Cerebellar ataxia, mental retardation, and dysequilibrium syndrome 4						False	3	0;0;0	0.109	False		ENSG00000132932	ENSG00000132932	HGNC:13533													
ATP8B1	gene	ATP8B1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Cholestasis, progressive familial intrahepatic 1, 211600 (3)						False	3	0;0;0	0.109	False		ENSG00000081923	ENSG00000081923	HGNC:3706													
ATR	gene	ATR	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Seckel syndrome 1, 210600 (3)						False	3	0;0;0	0.109	False		ENSG00000175054	ENSG00000175054	HGNC:882													
ATRX	gene	ATRX	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	X-LINKED: hemizygous mutation in males, biallelic mutations in females	ATR-X-related syndrome MONDO:0016980						False	3	0;0;0	0.109	False		ENSG00000085224	ENSG00000085224	HGNC:886													
AUH	gene	AUH	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	3-methylglutaconic aciduria, type I, 250950 (3)						False	3	0;0;0	0.109	False		ENSG00000148090	ENSG00000148090	HGNC:890													
B3GALNT2	gene	B3GALNT2	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies, type A, 11, 615181 (3)						False	3	0;0;0	0.109	False		ENSG00000162885	ENSG00000162885	HGNC:28596													
B3GALT6	gene	B3GALT6	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Spondyloepimetaphyseal dysplasia with joint laxity, type 1, with or without fractures, 271640 (3)						False	3	0;0;0	0.109	False		ENSG00000176022	ENSG00000176022	HGNC:17978													
B3GAT3	gene	B3GAT3	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Multiple joint dislocations, short stature, craniofacial dysmorphism, and congenital heart defects, 245600 (3)						False	3	0;0;0	0.109	False		ENSG00000149541	ENSG00000149541	HGNC:923													
B3GLCT	gene	B3GLCT	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Peters-plus syndrome, 261540 (3)						False	3	0;0;0	0.109	False		ENSG00000187676	ENSG00000187676	HGNC:20207													
B4GALNT1	gene	B4GALNT1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Spastic paraplegia 26, autosomal recessive, 609195 (3)						False	3	0;0;0	0.109	False		ENSG00000135454	ENSG00000135454	HGNC:4117													
B4GALT7	gene	B4GALT7	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Ehlers-Danlos syndrome, progeroid type, 1, 130070 (3)						False	3	0;0;0	0.109	False		ENSG00000027847	ENSG00000027847	HGNC:930													
BBS1	gene	BBS1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Bardet-Biedl syndrome 1, 209900 (3)						False	3	0;0;0	0.109	False		ENSG00000174483	ENSG00000174483	HGNC:966													
BBS10	gene	BBS10	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Bardet-Biedl syndrome 10, 615987 (3)						False	3	0;0;0	0.109	False		ENSG00000179941	ENSG00000179941	HGNC:26291													
BBS12	gene	BBS12	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Bardet-Biedl syndrome 12, 615989 (3)						False	3	0;0;0	0.109	False		ENSG00000181004	ENSG00000181004	HGNC:26648													
BBS2	gene	BBS2	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Bardet-Biedl syndrome 2, 615981 (3)						False	3	0;0;0	0.109	False		ENSG00000125124	ENSG00000125124	HGNC:967													
BBS4	gene	BBS4	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Bardet-Biedl syndrome 4, 615982 (3)						False	3	0;0;0	0.109	False		ENSG00000140463	ENSG00000140463	HGNC:969													
BBS5	gene	BBS5	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Bardet-Biedl syndrome 5, 615983 (3)						False	3	0;0;0	0.109	False		ENSG00000163093	ENSG00000163093	HGNC:970													
BBS7	gene	BBS7	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Bardet-Biedl syndrome 7, 615984 (3)						False	3	0;0;0	0.109	False		ENSG00000138686	ENSG00000138686	HGNC:18758													
BBS9	gene	BBS9	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Bardet-Biedl syndrome 9, 615986 (3)						False	3	0;0;0	0.109	False		ENSG00000122507	ENSG00000122507	HGNC:30000													
BCKDHA	gene	BCKDHA	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Maple syrup urine disease, type Ia, 248600 (3)						False	3	0;0;0	0.109	False		ENSG00000248098	ENSG00000248098	HGNC:986													
BCKDHB	gene	BCKDHB	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Maple syrup urine disease, type Ib, 248600 (3)						False	3	0;0;0	0.109	False		ENSG00000083123	ENSG00000083123	HGNC:987													
BCKDK	gene	BCKDK	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Branched-chain ketoacid dehydrogenase kinase deficiency, 614923 (3)						False	3	0;0;0	0.109	False		ENSG00000103507	ENSG00000103507	HGNC:16902													
BCS1L	gene	BCS1L	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	GRACILE syndrome, 603358 (3)						False	3	0;0;0	0.109	False		ENSG00000074582	ENSG00000074582	HGNC:1020													
BGN	gene	BGN	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	X-LINKED: hemizygous mutation in males, biallelic mutations in females	Meester-Loeys syndrome, 300989 (3), X-linked						False	3	0;0;0	0.109	False		ENSG00000182492	ENSG00000182492	HGNC:1044													
BIN1	gene	BIN1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Myopathy, centronuclear, autosomal recessive, 255200 (3)						False	3	0;0;0	0.109	False		ENSG00000136717	ENSG00000136717	HGNC:1052													
BLM	gene	BLM	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Bloom syndrome, 210900 (3)						False	3	0;0;0	0.109	False		ENSG00000197299	ENSG00000197299	HGNC:1058													
BMPER	gene	BMPER	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Diaphanospondylodysostosis, 608022 (3)						False	3	0;0;0	0.109	False		ENSG00000164619	ENSG00000164619	HGNC:24154													
BMPR1B	gene	BMPR1B	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Acromesomelic dysplasia, Demirhan type, 609441 (3), Autosomal recessive						False	3	0;0;0	0.109	False		ENSG00000138696	ENSG00000138696	HGNC:1077													
BOLA3	gene	BOLA3	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Multiple mitochondrial dysfunctions syndrome 2, 614299 (3)						False	3	0;0;0	0.109	False		ENSG00000163170	ENSG00000163170	HGNC:24415													
BRAT1	gene	BRAT1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Rigidity and multifocal seizure syndrome, lethal neonatal, 614498 (3)						False	3	0;0;0	0.109	False		ENSG00000106009	ENSG00000106009	HGNC:21701													
BRF1	gene	BRF1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Cerebellofaciodental syndrome, 616202 (3)						False	3	0;0;0	0.109	False		ENSG00000185024	ENSG00000185024	HGNC:11551													
BRWD3	gene	BRWD3	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	X-LINKED: hemizygous mutation in males, biallelic mutations in females	Mental retardation, X-linked 93, 300659 (3)						False	3	0;0;0	0.109	False		ENSG00000165288	ENSG00000165288	HGNC:17342													
BSCL2	gene	BSCL2	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Encephalopathy, progressive, with or without lipodystrophy, 615924 (3)						False	3	0;0;0	0.109	False		ENSG00000168000	ENSG00000168000	HGNC:15832													
BSND	gene	BSND	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Bartter syndrome, type 4a, 602522 (3)						False	3	0;0;0	0.109	False		ENSG00000162399	ENSG00000162399	HGNC:16512													
BTK	gene	BTK	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	X-LINKED: hemizygous mutation in males, biallelic mutations in females	Agammaglobulinemia and isolated hormone deficiency, 307200 (3)						False	3	0;0;0	0.109	False		ENSG00000010671	ENSG00000010671	HGNC:1133													
BUB1B	gene	BUB1B	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Mosaic variegated aneuploidy syndrome 1, 257300 (3)						False	3	0;0;0	0.109	False		ENSG00000156970	ENSG00000156970	HGNC:1149													
C12orf57	gene	C12orf57	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Temtamy syndrome, 218340 (3)						False	3	0;0;0	0.109	False		ENSG00000111678	ENSG00000111678	HGNC:29521													
C12orf65	gene	C12orf65	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Combined oxidative phosphorylation deficiency 7, 613559 (3)						False	3	0;0;0	0.109	False		ENSG00000130921	ENSG00000130921	HGNC:26784													
C19orf12	gene	C19orf12	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Neurodegeneration with brain iron accumulation 4, 614298 (3)						False	3	0;0;0	0.109	False		ENSG00000131943	ENSG00000131943	HGNC:25443													
C1QA	gene	C1QA	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	C1q deficiency, 613652 (3)						False	3	0;0;0	0.109	False		ENSG00000173372	ENSG00000173372	HGNC:1241													
C1QB	gene	C1QB	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	C1q deficiency, 613652 (3)						False	3	0;0;0	0.109	False		ENSG00000173369	ENSG00000173369	HGNC:1242													
C1QC	gene	C1QC	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	C1q deficiency, 613652 (3)						False	3	0;0;0	0.109	False		ENSG00000159189	ENSG00000159189	HGNC:1245													
C21orf2	gene	C21orf2	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Retinal dystrophy with macular staphyloma, 617547 (3), Autosomal recessive						False	3	0;0;0	0.109	False		ENSG00000160226	ENSG00000160226	HGNC:1260													
C2CD3	gene	C2CD3	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Orofaciodigital syndrome XIV						False	3	0;0;0	0.109	False		ENSG00000168014	ENSG00000168014	HGNC:24564													
C3	gene	C3	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	C3 deficiency, 613779 (3)						False	3	0;0;0	0.109	False		ENSG00000125730	ENSG00000125730	HGNC:1318													
C5	gene	C5	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	C5 deficiency, 609536 (3)						False	3	0;0;0	0.109	False		ENSG00000106804	ENSG00000106804	HGNC:1331													
C5orf42	gene	C5orf42	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Joubert syndrome 17, 614615 (3)						False	3	0;0;0	0.109	False		ENSG00000197603	ENSG00000197603	HGNC:25801													
C6	gene	C6	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	C6 deficiency, 612446 (3)						False	3	0;0;0	0.109	False		ENSG00000039537	ENSG00000039537	HGNC:1339													
C7	gene	C7	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	C7 deficiency, 610102 (3)						False	3	0;0;0	0.109	False		ENSG00000112936	ENSG00000112936	HGNC:1346													
C8B	gene	C8B	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	C8 deficiency, type II, 613789 (3)						False	3	0;0;0	0.109	False		ENSG00000021852	ENSG00000021852	HGNC:1353													
C8orf37	gene	C8orf37	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Cone-rod dystrophy 16, 614500 (3)						False	3	0;0;0	0.109	False		ENSG00000156172	ENSG00000156172	HGNC:27232													
CA2	gene	CA2	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Osteopetrosis, autosomal recessive 3, with renal tubular acidosis, 259730 (3)						False	3	0;0;0	0.109	False		ENSG00000104267	ENSG00000104267	HGNC:1373													
CABP4	gene	CABP4	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Cone-rod synaptic disorder, congenital nonprogressive, 610427 (3)						False	3	0;0;0	0.109	False		ENSG00000175544	ENSG00000175544	HGNC:1386													
CANT1	gene	CANT1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Desbuquois dysplasia, 251450 (3)						False	3	0;0;0	0.109	False		ENSG00000171302	ENSG00000171302	HGNC:19721													
CAPN3	gene	CAPN3	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Muscular dystrophy, limb-girdle, type 2A, 253600 (3)						False	3	0;0;0	0.109	False		ENSG00000092529	ENSG00000092529	HGNC:1480													
CARD11	gene	CARD11	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Immunodeficiency 11, 615206 (3)						False	3	0;0;0	0.109	False		ENSG00000198286	ENSG00000198286	HGNC:16393													
CARD9	gene	CARD9	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Candidiasis, familial, 2, autosomal recessive, 212050 (3)						False	3	0;0;0	0.109	False		ENSG00000187796	ENSG00000187796	HGNC:16391													
CARS2	gene	CARS2	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Combined oxidative phosphorylation deficiency 27, 616672 (3), Autosomal recessive						False	3	0;0;0	0.109	False		ENSG00000134905	ENSG00000134905	HGNC:25695													
CASK	gene	CASK	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	X-LINKED: hemizygous mutation in males, biallelic mutations in females	Mental retardation, with or without nystagmus						False	3	0;0;0	0.109	False		ENSG00000147044	ENSG00000147044	HGNC:1497													
CASQ2	gene	CASQ2	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Ventricular tachycardia, catecholaminergic polymorphic, 2, 611938 (3)						False	3	0;0;0	0.109	False		ENSG00000118729	ENSG00000118729	HGNC:1513													
CASR	gene	CASR	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Hyperparathyroidism, neonatal, 239200 (3)						False	3	0;0;0	0.109	False		ENSG00000036828	ENSG00000036828	HGNC:1514													
CAVIN1	gene	CAVIN1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Lipodystrophy, congenital generalized, type 4, 613327 (3)						False	3	0;0;0	0.109	False		ENSG00000177469	ENSG00000177469	HGNC:9688													
CC2D1A	gene	CC2D1A	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Mental retardation, autosomal recessive 3, 608443 (3)						False	3	0;0;0	0.109	False		ENSG00000132024	ENSG00000132024	HGNC:30237													
CC2D2A	gene	CC2D2A	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Joubert syndrome 9, 612285 (3)						False	3	0;0;0	0.109	False		ENSG00000048342	ENSG00000048342	HGNC:29253													
CCBE1	gene	CCBE1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Hennekam lymphangiectasia-lymphedema syndrome 1, 235510 (3)						False	3	0;0;0	0.109	False		ENSG00000183287	ENSG00000183287	HGNC:29426													
CCDC103	gene	CCDC103	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Ciliary dyskinesia, primary, 17, 614679 (3)						False	3	0;0;0	0.109	False		ENSG00000167131	ENSG00000167131	HGNC:32700													
CCDC114	gene	CCDC114	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Ciliary dyskinesia, primary, 20, 615067 (3)						False	3	0;0;0	0.109	False		ENSG00000105479	ENSG00000105479	HGNC:26560													
CCDC115	gene	CCDC115	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Congenital disorder of glycosylation, type IIo, 616828 (3), Autosomal recessive						False	3	0;0;0	0.109	False		ENSG00000136710	ENSG00000136710	HGNC:28178													
CCDC39	gene	CCDC39	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Ciliary dyskinesia, primary, 14, 613807 (3)						False	3	0;0;0	0.109	False		ENSG00000145075	ENSG00000145075	HGNC:25244													
CCDC40	gene	CCDC40	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Ciliary dyskinesia, primary, 15, 613808 (3)						False	3	0;0;0	0.109	False		ENSG00000141519	ENSG00000141519	HGNC:26090													
CCDC8	gene	CCDC8	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	3-M syndrome 3, 614205 (3)						False	3	0;0;0	0.109	False		ENSG00000169515	ENSG00000169515	HGNC:25367													
CCDC88C	gene	CCDC88C	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Hydrocephalus, nonsyndromic, autosomal recessive, 236600 (3)						False	3	0;0;0	0.109	False		ENSG00000015133	ENSG00000015133	HGNC:19967													
CCNO	gene	CCNO	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Ciliary diskinesia, primary, 29, 615872 (3)						False	3	0;0;0	0.109	False		ENSG00000152669	ENSG00000152669	HGNC:18576													
CD27	gene	CD27	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Lymphoproliferative syndrome 2, 615122 (3)						False	3	0;0;0	0.109	False		ENSG00000139193	ENSG00000139193	HGNC:11922													
CD3D	gene	CD3D	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Immunodeficiency 19, 615617 (3)						False	3	0;0;0	0.109	False		ENSG00000167286	ENSG00000167286	HGNC:1673													
CD40	gene	CD40	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Immunodeficiency with hyper-IgM, type 3, 606843 (3)						False	3	0;0;0	0.109	False		ENSG00000101017	ENSG00000101017	HGNC:11919													
CD40LG	gene	CD40LG	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	X-LINKED: hemizygous mutation in males, biallelic mutations in females	Immunodeficiency, X-linked, with hyper-IgM, 308230 (3)						False	3	0;0;0	0.109	False		ENSG00000102245	ENSG00000102245	HGNC:11935													
CD55	gene	CD55	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Complement hyperactivation, angiopathic thrombosis, and protein-losing enteropathy, 226300 (3), Autosomal recessive						False	3	0;0;0	0.109	False		ENSG00000196352	ENSG00000196352	HGNC:2665													
CDC45	gene	CDC45	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Meier-Gorlin syndrome 7, 617063 (3), Autosomal recessive						False	3	0;0;0	0.109	False		ENSG00000093009	ENSG00000093009	HGNC:1739													
CDH11	gene	CDH11	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Elsahy-Waters syndrome, 211380 (3), Autosomal recessive						False	3	0;0;0	0.109	False		ENSG00000140937	ENSG00000140937	HGNC:1750													
CDH23	gene	CDH23	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Usher syndrome, type 1D, 601067 (3)						False	3	0;0;0	0.109	False		ENSG00000107736	ENSG00000107736	HGNC:13733													
CDH3	gene	CDH3	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Ectodermal dysplasia, ectrodactyly, and macular dystrophy, 225280 (3)						False	3	0;0;0	0.109	False		ENSG00000062038	ENSG00000062038	HGNC:1762													
CDK10	gene	CDK10	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Al Kaissi syndrome, 617694 (3), Autosomal recessive						False	3	0;0;0	0.109	False		ENSG00000185324	ENSG00000185324	HGNC:1770													
CDK5RAP2	gene	CDK5RAP2	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Microcephaly 3, primary, autosomal recessive, 604804 (3)						False	3	0;0;0	0.109	False		ENSG00000136861	ENSG00000136861	HGNC:18672													
CDT1	gene	CDT1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Meier-Gorlin syndrome 4, 613804 (3)						False	3	0;0;0	0.109	False		ENSG00000167513	ENSG00000167513	HGNC:24576													
CENPJ	gene	CENPJ	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Microcephaly 6, primary, autosomal recessive, 608393 (3)						False	3	0;0;0	0.109	False		ENSG00000151849	ENSG00000151849	HGNC:17272													
CEP120	gene	CEP120	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Short-rib thoracic dysplasia 13 with or without polydactyly, 616300 (3)						False	3	0;0;0	0.109	False		ENSG00000168944	ENSG00000168944	HGNC:26690													
CEP152	gene	CEP152	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Seckel syndrome 5, 613823 (3)						False	3	0;0;0	0.109	False		ENSG00000103995	ENSG00000103995	HGNC:29298													
CEP290	gene	CEP290	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Joubert syndrome 5, 610188 (3)						False	3	0;0;0	0.109	False		ENSG00000198707	ENSG00000198707	HGNC:29021													
CEP41	gene	CEP41	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Joubert syndrome 15, 614464 (3)						False	3	0;0;0	0.109	False		ENSG00000106477	ENSG00000106477	HGNC:12370													
CEP78	gene	CEP78	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Cone-rod dystrophy and hearing loss, 617236 (3), Autosomal recessive						False	3	0;0;0	0.109	False		ENSG00000148019	ENSG00000148019	HGNC:25740													
CERS3	gene	CERS3	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Ichthyosis, congenital, autosomal recessive 9, 615023 (3)						False	3	0;0;0	0.109	False		ENSG00000154227	ENSG00000154227	HGNC:23752													
CFD	gene	CFD	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Complement factor D deficiency, 613912 (3)						False	3	0;0;0	0.109	False		ENSG00000197766	ENSG00000197766	HGNC:2771													
CFH	gene	CFH	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Complement factor H deficiency, 609814 (3)						False	3	0;0;0	0.109	False		ENSG00000000971	ENSG00000000971	HGNC:4883													
CFI	gene	CFI	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Complement factor I deficiency, 610984 (3)						False	3	0;0;0	0.109	False		ENSG00000205403	ENSG00000205403	HGNC:5394													
CFL2	gene	CFL2	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Nemaline myopathy 7, autosomal recessive, 610687 (3)						False	3	0;0;0	0.109	False		ENSG00000165410	ENSG00000165410	HGNC:1875													
CFP	gene	CFP	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	X-LINKED: hemizygous mutation in males, biallelic mutations in females	Properdin deficiency, X-linked, 312060 (3)						False	3	0;0;0	0.109	False		ENSG00000126759	ENSG00000126759	HGNC:8864													
CFTR	gene	CFTR	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Cystic fibrosis, 219700 (3)						False	3	0;0;0	0.109	False		ENSG00000001626	ENSG00000001626	HGNC:1884													
CHAT	gene	CHAT	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Myasthenic syndrome, congenital, 6, presynaptic, 254210 (3)						False	3	0;0;0	0.109	False		ENSG00000070748	ENSG00000070748	HGNC:1912													
CHKB	gene	CHKB	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Muscular dystrophy, congenital, megaconial type, 602541 (3)						False	3	0;0;0	0.109	False		ENSG00000100288	ENSG00000100288	HGNC:1938													
CHM	gene	CHM	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	X-LINKED: hemizygous mutation in males, biallelic mutations in females	Choroideremia						False	3	0;0;0	0.109	False		ENSG00000188419	ENSG00000188419	HGNC:1940													
CHRNA1	gene	CHRNA1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Multiple pterygium syndrome, lethal type, 253290 (3)						False	3	0;0;0	0.109	False		ENSG00000138435	ENSG00000138435	HGNC:1955													
CHRND	gene	CHRND	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Myasthenic syndrome, congenital, 3B, fast-channel, 616322 (3)						False	3	0;0;0	0.109	False		ENSG00000135902	ENSG00000135902	HGNC:1965													
CHRNE	gene	CHRNE	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Myasthenic syndrome, congenital, 4A, slow-channel, 605809 (3)						False	3	0;0;0	0.109	False		ENSG00000108556	ENSG00000108556	HGNC:1966													
CHRNG	gene	CHRNG	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Escobar syndrome, 265000 (3)						False	3	0;0;0	0.109	False		ENSG00000196811	ENSG00000196811	HGNC:1967													
CHST14	gene	CHST14	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Ehlers-Danlos syndrome, musculocontractural type 1, 601776 (3)						False	3	0;0;0	0.109	False		ENSG00000169105	ENSG00000169105	HGNC:24464													
CHST3	gene	CHST3	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Spondyloepiphyseal dysplasia with congenital joint dislocations, 143095 (3)						False	3	0;0;0	0.109	False		ENSG00000122863	ENSG00000122863	HGNC:1971													
CHSY1	gene	CHSY1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Temtamy preaxial brachydactyly syndrome, 605282 (3)						False	3	0;0;0	0.109	False		ENSG00000131873	ENSG00000131873	HGNC:17198													
CIITA	gene	CIITA	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Bare lymphocyte syndrome, type II, complementation group A, 209920 (3)						False	3	0;0;0	0.109	False		ENSG00000179583	ENSG00000179583	HGNC:7067													
CISD2	gene	CISD2	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Wolfram syndrome 2, 604928 (3)						False	3	0;0;0	0.109	False		ENSG00000145354	ENSG00000145354	HGNC:24212													
CIT	gene	CIT	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Microcephaly 17, primary, autosomal recessive, 617090 (3)						False	3	0;0;0	0.109	False		ENSG00000122966	ENSG00000122966	HGNC:1985													
CKAP2L	gene	CKAP2L	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Filippi syndrome, 272440 (3)						False	3	0;0;0	0.109	False		ENSG00000169607	ENSG00000169607	HGNC:26877													
CLCF1	gene	CLCF1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Cold-induced sweating syndrome 2, 610313 (3)						False	3	0;0;0	0.109	False		ENSG00000175505	ENSG00000175505	HGNC:17412													
CLCN2	gene	CLCN2	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Leukoencephalopathy with ataxia, 615651 (3)						False	3	0;0;0	0.109	False		ENSG00000114859	ENSG00000114859	HGNC:2020													
CLCN4	gene	CLCN4	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)	Raynaud-Claes syndrome, MIM #300114				27550844		False	3	100;0;0	0.109	True		ENSG00000073464	ENSG00000073464	HGNC:2022													
CLCN5	gene	CLCN5	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	X-LINKED: hemizygous mutation in males, biallelic mutations in females	Dent disease, 300009 (3)						False	3	0;0;0	0.109	False		ENSG00000171365	ENSG00000171365	HGNC:2023													
CLCN7	gene	CLCN7	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Osteopetrosis, autosomal recessive 4, 611490 (3)						False	3	0;0;0	0.109	False		ENSG00000103249	ENSG00000103249	HGNC:2025													
CLCNKB	gene	CLCNKB	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Bartter syndrome, type 4b, digenic, 613090 (3)						False	3	0;0;0	0.109	False		ENSG00000184908	ENSG00000184908	HGNC:2027													
CLDN1	gene	CLDN1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Ichthyosis, leukocyte vacuoles, alopecia, and sclerosing cholangitis, 607626 (3)						False	3	0;0;0	0.109	False		ENSG00000163347	ENSG00000163347	HGNC:2032													
CLDN10	gene	CLDN10	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	HELIX syndrome, 617671 (3), Autosomal recessive						False	3	0;0;0	0.109	False		ENSG00000134873	ENSG00000134873	HGNC:2033													
CLDN19	gene	CLDN19	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Hypomagnesemia 5, renal, with ocular involvement, 248190 (3)						False	3	0;0;0	0.109	False		ENSG00000164007	ENSG00000164007	HGNC:2040													
CLMP	gene	CLMP	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Congenital short bowel syndrome, 615237 (3)						False	3	0;0;0	0.109	False		ENSG00000166250	ENSG00000166250	HGNC:24039													
CLN3	gene	CLN3	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Ceroid lipofuscinosis, neuronal, 3, 204200 (3)						False	3	0;0;0	0.109	False		ENSG00000188603	ENSG00000188603	HGNC:2074													
CLN5	gene	CLN5	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Ceroid lipofuscinosis, neuronal, 5, 256731 (3)						False	3	0;0;0	0.109	False		ENSG00000102805	ENSG00000102805	HGNC:2076													
CLN6	gene	CLN6	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Ceroid lipofuscinosis, neuronal 6, 601780 (3)						False	3	0;0;0	0.109	False		ENSG00000128973	ENSG00000128973	HGNC:2077													
CLN8	gene	CLN8	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Ceroid lipofuscinosis, neuronal, 8, 600143 (3)						False	3	0;0;0	0.109	False		ENSG00000182372	ENSG00000182372	HGNC:2079													
CLP1	gene	CLP1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Pontocerebellar hypoplasia, type 10, 615803 (3)						False	3	0;0;0	0.109	False		ENSG00000172409	ENSG00000172409	HGNC:16999													
CLPB	gene	CLPB	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	3-methylglutaconic aciduria, type VII, with cataracts, neurologic involvement and neutropenia, 616271 (3)						False	3	0;0;0	0.109	False		ENSG00000162129	ENSG00000162129	HGNC:30664													
CLPP	gene	CLPP	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Perrault syndrome 3, 614129 (3)						False	3	0;0;0	0.109	False		ENSG00000125656	ENSG00000125656	HGNC:2084													
CLRN1	gene	CLRN1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Usher syndrome, type 3A, 276902 (3)						False	3	0;0;0	0.109	False		ENSG00000163646	ENSG00000163646	HGNC:12605													
CNGA3	gene	CNGA3	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Achromatopsia-2, 216900 (3)						False	3	0;0;0	0.109	False		ENSG00000144191	ENSG00000144191	HGNC:2150													
CNGB3	gene	CNGB3	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Macular degeneration, juvenile, 248200 (3)						False	3	0;0;0	0.109	False		ENSG00000170289	ENSG00000170289	HGNC:2153													
CNNM4	gene	CNNM4	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Jalili syndrome, 217080 (3)						False	3	0;0;0	0.109	False		ENSG00000158158	ENSG00000158158	HGNC:105													
CNTNAP1	gene	CNTNAP1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Lethal congenital contracture syndrome 7, 616286 (3)						False	3	0;0;0	0.109	False		ENSG00000108797	ENSG00000108797	HGNC:8011													
CNTNAP2	gene	CNTNAP2	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Cortical dysplasia-focal epilepsy syndrome, 610042 (3)						False	3	0;0;0	0.109	False		ENSG00000174469	ENSG00000174469	HGNC:13830													
COG6	gene	COG6	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Congenital disorder of glycosylation, type IIl, 614576 (3)						False	3	0;0;0	0.109	False		ENSG00000133103	ENSG00000133103	HGNC:18621													
COG7	gene	COG7	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Congenital disorder of glycosylation, type IIe, 608779 (3)						False	3	0;0;0	0.109	False		ENSG00000168434	ENSG00000168434	HGNC:18622													
COL11A1	gene	COL11A1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Fibrochondrogenesis 1, 228520 (3)						False	3	0;0;0	0.109	False		ENSG00000060718	ENSG00000060718	HGNC:2186													
COL11A2	gene	COL11A2	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Fibrochondrogenesis 2, 614524 (3)						False	3	0;0;0	0.109	False		ENSG00000204248	ENSG00000204248	HGNC:2187													
COL17A1	gene	COL17A1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Epidermolysis bullosa, junctional, non-Herlitz type, 226650 (3)						False	3	0;0;0	0.109	False		ENSG00000065618	ENSG00000065618	HGNC:2194													
COL18A1	gene	COL18A1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Knobloch syndrome, type 1, 267750 (3)						False	3	0;0;0	0.109	False		ENSG00000182871	ENSG00000182871	HGNC:2195													
COL27A1	gene	COL27A1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Steel Syndrome						False	3	0;0;0	0.109	False		ENSG00000196739	ENSG00000196739	HGNC:22986													
COL4A3	gene	COL4A3	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Alport syndrome, autosomal recessive, 203780 (3)						False	3	0;0;0	0.109	False		ENSG00000169031	ENSG00000169031	HGNC:2204													
COL4A4	gene	COL4A4	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Alport syndrome, autosomal recessive, 203780 (3)						False	3	0;0;0	0.109	False		ENSG00000081052	ENSG00000081052	HGNC:2206													
COL4A5	gene	COL4A5	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)	Alport syndrome 1, X-linked						False	3	0;0;0	0.109	True		ENSG00000188153	ENSG00000188153	HGNC:2207													
COL6A1	gene	COL6A1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Ullrich congenital muscular dystrophy 1, 254090 (3)						False	3	0;0;0	0.109	False		ENSG00000142156	ENSG00000142156	HGNC:2211													
COL6A2	gene	COL6A2	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Ullrich congenital muscular dystrophy 1, 254090 (3)						False	3	0;0;0	0.109	False		ENSG00000142173	ENSG00000142173	HGNC:2212													
COL6A3	gene	COL6A3	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Ullrich congenital muscular dystrophy 1, 254090 (3)						False	3	0;0;0	0.109	False		ENSG00000163359	ENSG00000163359	HGNC:2213													
COL7A1	gene	COL7A1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Epidermolysis bullosa dystrophica, AR, 226600 (3)						False	3	0;0;0	0.109	False		ENSG00000114270	ENSG00000114270	HGNC:2214													
COLEC11	gene	COLEC11	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	3MC syndrome 2, 265050 (3)						False	3	0;0;0	0.109	False		ENSG00000118004	ENSG00000118004	HGNC:17213													
COLQ	gene	COLQ	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Myasthenic syndrome, congenital, 5, 603034 (3)						False	3	0;0;0	0.109	False		ENSG00000206561	ENSG00000206561	HGNC:2226													
COQ2	gene	COQ2	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Coenzyme Q10 deficiency, primary, 1, 607426 (3)						False	3	0;0;0	0.109	False		ENSG00000173085	ENSG00000173085	HGNC:25223													
COQ4	gene	COQ4	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Coenzyme Q10 deficiency, primary, 7, 616276 (3)						False	3	0;0;0	0.109	False		ENSG00000167113	ENSG00000167113	HGNC:19693													
COQ6	gene	COQ6	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Coenzyme Q10 deficiency, primary, 6, 614650 (3)						False	3	0;0;0	0.109	False		ENSG00000119723	ENSG00000119723	HGNC:20233													
COQ8A	gene	COQ8A	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Coenzyme Q10 deficiency, primary, 4, 612016 (3)						False	3	0;0;0	0.109	False		ENSG00000163050	ENSG00000163050	HGNC:16812													
COQ8B	gene	COQ8B	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Nephrotic syndrome, type 9, 615573 (3)						False	3	0;0;0	0.109	False		ENSG00000123815	ENSG00000123815	HGNC:19041													
COX10	gene	COX10	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Leigh syndrome due to mitochondrial COX4 deficiency, 256000 (3)						False	3	0;0;0	0.109	False		ENSG00000006695	ENSG00000006695	HGNC:2260													
COX15	gene	COX15	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency 2, 615119 (3)						False	3	0;0;0	0.109	False		ENSG00000014919	ENSG00000014919	HGNC:2263													
COX20	gene	COX20	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Mitochondrial complex IV deficiency, 220110 (3)						False	3	0;0;0	0.109	False		ENSG00000203667	ENSG00000203667	HGNC:26970													
CPS1	gene	CPS1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Carbamoylphosphate synthetase I deficiency, 237300 (3)						False	3	0;0;0	0.109	False		ENSG00000021826	ENSG00000021826	HGNC:2323													
CPT1A	gene	CPT1A	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	CPT deficiency, hepatic, type IA, 255120 (3)						False	3	0;0;0	0.109	False		ENSG00000110090	ENSG00000110090	HGNC:2328													
CPT2	gene	CPT2	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	CPT II deficiency, lethal neonatal, 608836 (3)						False	3	0;0;0	0.109	False		ENSG00000157184	ENSG00000157184	HGNC:2330													
CRB1	gene	CRB1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Leber congenital amaurosis 8, 613835 (3)						False	3	0;0;0	0.109	False		ENSG00000134376	ENSG00000134376	HGNC:2343													
CRB2	gene	CRB2	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Ventriculomegaly with cystic kidney disease, 219730 (3)						False	3	0;0;0	0.109	False		ENSG00000148204	ENSG00000148204	HGNC:18688													
CRLF1	gene	CRLF1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Cold-induced sweating syndrome 1, 272430 (3)						False	3	0;0;0	0.109	False		ENSG00000006016	ENSG00000006016	HGNC:2364													
CRTAP	gene	CRTAP	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Osteogenesis imperfecta, type VII, 610682 (3)						False	3	0;0;0	0.109	False		ENSG00000170275	ENSG00000170275	HGNC:2379													
CSPP1	gene	CSPP1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Joubert syndrome 21, 615636 (3)						False	3	0;0;0	0.109	False		ENSG00000104218	ENSG00000104218	HGNC:26193													
CSTB	gene	CSTB	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Epilepsy, progressive myoclonic 1A (Unverricht and Lundborg), 254800 (3)						False	3	100;0;0	0.109	False		ENSG00000160213	ENSG00000160213	HGNC:2482													
CTC1	gene	CTC1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Cerebroretinal microangiopathy with calcifications and cysts, 612199 (3)						False	3	0;0;0	0.109	False		ENSG00000178971	ENSG00000178971	HGNC:26169													
CTNS	gene	CTNS	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Cystinosis, nephropathic, 219800 (3)						False	3	0;0;0	0.109	False		ENSG00000040531	ENSG00000040531	HGNC:2518													
CTPS1	gene	CTPS1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Immunodeficiency 24, 615897 (3)						False	3	0;0;0	0.109	False		ENSG00000171793	ENSG00000171793	HGNC:2519													
CTSA	gene	CTSA	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Galactosialidosis, 256540 (3)						False	3	0;0;0	0.109	False		ENSG00000064601	ENSG00000064601	HGNC:9251													
CTSC	gene	CTSC	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Papillon-Lefevre syndrome, 245000 (3)						False	3	0;0;0	0.109	False		ENSG00000109861	ENSG00000109861	HGNC:2528													
CTSD	gene	CTSD	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Ceroid lipofuscinosis, neuronal, 10, 610127 (3)						False	3	0;0;0	0.109	False		ENSG00000117984	ENSG00000117984	HGNC:2529													
CTSF	gene	CTSF	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Ceroid lipofuscinosis, neuronal, 13, Kufs type, 615362 (3)						False	3	0;0;0	0.109	False		ENSG00000174080	ENSG00000174080	HGNC:2531													
CTSK	gene	CTSK	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Pycnodysostosis, 265800 (3)						False	3	0;0;0	0.109	False		ENSG00000143387	ENSG00000143387	HGNC:2536													
CUL4B	gene	CUL4B	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	X-LINKED: hemizygous mutation in males, biallelic mutations in females	Mental retardation, X-linked, syndromic 15 (Cabezas type), 300354 (3)						False	3	0;0;0	0.109	False		ENSG00000158290	ENSG00000158290	HGNC:2555													
CUL7	gene	CUL7	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	3-M syndrome 1, 273750 (3)						False	3	0;0;0	0.109	False		ENSG00000044090	ENSG00000044090	HGNC:21024													
CWC27	gene	CWC27	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Retinitis pigmentosa with or without skeletal anomalies, 250410 (3), Autosomal recessive						False	3	0;0;0	0.109	False		ENSG00000153015	ENSG00000153015	HGNC:10664													
CYB5R3	gene	CYB5R3	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Methemoglobinemia, type I, 250800 (3)						False	3	0;0;0	0.109	False		ENSG00000100243	ENSG00000100243	HGNC:2873													
CYBA	gene	CYBA	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Chronic granulomatous disease, autosomal, due to deficiency of CYBA, 233690 (3)						False	3	0;0;0	0.109	False		ENSG00000051523	ENSG00000051523	HGNC:2577													
CYBB	gene	CYBB	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	X-LINKED: hemizygous mutation in males, biallelic mutations in females	Chronic granulomatous disease, X-linked, 306400 (3)						False	3	0;0;0	0.109	False		ENSG00000165168	ENSG00000165168	HGNC:2578													
CYP11A1	gene	CYP11A1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Adrenal insufficiency, congenital, with 46XY sex reversal, partial or complete, 613743 (3)						False	3	0;0;0	0.109	False		ENSG00000140459	ENSG00000140459	HGNC:2590													
CYP11B2	gene	CYP11B2	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Hypoaldosteronism, congenital, due to CMO I deficiency, 203400 (3)						False	3	0;0;0	0.109	False		ENSG00000179142	ENSG00000179142	HGNC:2592													
CYP17A1	gene	CYP17A1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	17,20-lyase deficiency, isolated, 202110 (3)						False	3	0;0;0	0.109	False		ENSG00000148795	ENSG00000148795	HGNC:2593													
CYP1B1	gene	CYP1B1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Glaucoma 3A, primary open angle, congenital, juvenile, or adult onset, 231300 (3)						False	3	0;0;0	0.109	False		ENSG00000138061	ENSG00000138061	HGNC:2597													
CYP27A1	gene	CYP27A1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Cerebrotendinous xanthomatosis, 213700 (3)						False	3	0;0;0	0.109	False		ENSG00000135929	ENSG00000135929	HGNC:2605													
CYP2U1	gene	CYP2U1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Spastic paraplegia 56, autosomal recessive, 615030 (3)						False	3	0;0;0	0.109	False		ENSG00000155016	ENSG00000155016	HGNC:20582													
CYP4F22	gene	CYP4F22	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Ichthyosis, congenital, autosomal recessive 5, 604777 (3)						False	3	0;0;0	0.109	False		ENSG00000171954	ENSG00000171954	HGNC:26820													
CYP7B1	gene	CYP7B1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Bile acid synthesis defect, congenital, 3, 613812 (3)						False	3	0;0;0	0.109	False		ENSG00000172817	ENSG00000172817	HGNC:2652													
D2HGDH	gene	D2HGDH	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	D-2-hydroxyglutaric aciduria, 600721 (3)						False	3	0;0;0	0.109	False		ENSG00000180902	ENSG00000180902	HGNC:28358													
DARS	gene	DARS	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Hypomyelination with brainstem and spinal cord involvement and leg spasticity, 615281 (3)						False	3	100;0;0	0.109	True		ENSG00000115866	ENSG00000115866	HGNC:2678													
DARS2	gene	DARS2	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Leukoencephalopathy with brain stem and spinal cord involvement and lactate elevation, 611105 (3)						False	3	0;0;0	0.109	False		ENSG00000117593	ENSG00000117593	HGNC:25538													
DBT	gene	DBT	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Maple syrup urine disease, type II, 248600 (3)						False	3	0;0;0	0.109	False		ENSG00000137992	ENSG00000137992	HGNC:2698													
DCAF17	gene	DCAF17	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Woodhouse-Sakati syndrome, 241080 (3)						False	3	0;0;0	0.109	False		ENSG00000115827	ENSG00000115827	HGNC:25784													
DCDC2	gene	DCDC2	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Nephronophthisis 19, 616217 (3)						False	3	0;0;0	0.109	False		ENSG00000146038	ENSG00000146038	HGNC:18141													
DCHS1	gene	DCHS1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Van Maldergem syndrome 1, 601390 (3)						False	3	0;0;0	0.109	False		ENSG00000166341	ENSG00000166341	HGNC:13681													
DCLRE1C	gene	DCLRE1C	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Severe combined immunodeficiency, Athabascan type, 602450 (3)						False	3	0;0;0	0.109	False		ENSG00000152457	ENSG00000152457	HGNC:17642													
DCX	gene	DCX	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	X-LINKED: hemizygous mutation in males, biallelic mutations in females	Lissencephaly, X-linked, 300067 (3)						False	3	0;0;0	0.109	False		ENSG00000077279	ENSG00000077279	HGNC:2714													
DDC	gene	DDC	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Aromatic L-amino acid decarboxylase deficiency, 608643 (3)						False	3	0;0;0	0.109	False		ENSG00000132437	ENSG00000132437	HGNC:2719													
DDHD2	gene	DDHD2	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Spastic paraplegia 54, autosomal recessive, 615033 (3)						False	3	0;0;0	0.109	False		ENSG00000085788	ENSG00000085788	HGNC:29106													
DDR2	gene	DDR2	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Spondylometaepiphyseal dysplasia, short limb-hand type, 271665 (3)						False	3	0;0;0	0.109	False		ENSG00000162733	ENSG00000162733	HGNC:2731													
DDX11	gene	DDX11	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Warsaw breakage syndrome, 613398 (3)						False	3	0;0;0	0.109	False		ENSG00000013573	ENSG00000013573	HGNC:2736													
DDX59	gene	DDX59	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Orofaciodigital syndrome V, 174300 (3)						False	3	0;0;0	0.109	False		ENSG00000118197	ENSG00000118197	HGNC:25360													
DENND5A	gene	DENND5A	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Epileptic encephalopathy, early infantile, 49, 617281 (3), Autosomal recessive						False	3	0;0;0	0.109	False		ENSG00000184014	ENSG00000184014	HGNC:19344													
DGAT1	gene	DGAT1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	?Diarrhea 7, protein-losing enteropathy type						False	3	0;0;0	0.109	False		ENSG00000185000	ENSG00000185000	HGNC:2843													
DGKE	gene	DGKE	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Nephrotic syndrome, type 7, 615008 (3)						False	3	0;0;0	0.109	False		ENSG00000153933	ENSG00000153933	HGNC:2852													
DGUOK	gene	DGUOK	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Mitochondrial DNA depletion syndrome 3 (hepatocerebral type), 251880 (3)						False	3	0;0;0	0.109	False		ENSG00000114956	ENSG00000114956	HGNC:2858													
DHCR24	gene	DHCR24	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Desmosterolosis, 602398 (3)						False	3	0;0;0	0.109	False		ENSG00000116133	ENSG00000116133	HGNC:2859													
DHCR7	gene	DHCR7	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Smith-Lemli-Opitz syndrome, 270400 (3)						False	3	0;0;0	0.109	False		ENSG00000172893	ENSG00000172893	HGNC:2860													
DHDDS	gene	DHDDS	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Retinitis pigmentosa 59, 613861 (3)						False	3	0;0;0	0.109	False		ENSG00000117682	ENSG00000117682	HGNC:20603													
DHODH	gene	DHODH	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Miller syndrome, 263750 (3)						False	3	0;0;0	0.109	False		ENSG00000102967	ENSG00000102967	HGNC:2867													
DIS3L2	gene	DIS3L2	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Perlman syndrome, 267000 (3)						False	3	0;0;0	0.109	False		ENSG00000144535	ENSG00000144535	HGNC:28648													
DKC1	gene	DKC1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	X-LINKED: hemizygous mutation in males, biallelic mutations in females	Dyskeratosis congenita, X-linked, 305000 (3)						False	3	0;0;0	0.109	False		ENSG00000130826	ENSG00000130826	HGNC:2890													
DLD	gene	DLD	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Dihydrolipoamide dehydrogenase deficiency, 246900 (3)						False	3	0;0;0	0.109	False		ENSG00000091140	ENSG00000091140	HGNC:2898													
DLG3	gene	DLG3	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	X-LINKED: hemizygous mutation in males, biallelic mutations in females	Mental retardation, X-linked 90, 300850 (3)						False	3	0;0;0	0.109	False		ENSG00000082458	ENSG00000082458	HGNC:2902													
DLL3	gene	DLL3	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Spondylocostal dysostosis 1, autosomal recessive, 277300 (3)						False	3	0;0;0	0.109	False		ENSG00000090932	ENSG00000090932	HGNC:2909													
DMD	gene	DMD	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	X-LINKED: hemizygous mutation in males, biallelic mutations in females	Duchenne muscular dystrophy, 310200 (3)						False	3	0;0;0	0.109	False		ENSG00000198947	ENSG00000198947	HGNC:2928													
DNAAF1	gene	DNAAF1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Ciliary dyskinesia, primary, 13, 613193 (3)						False	3	0;0;0	0.109	False		ENSG00000154099	ENSG00000154099	HGNC:30539													
DNAAF3	gene	DNAAF3	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Ciliary dyskinesia, primary, 2, 606763 (3)						False	3	0;0;0	0.109	False		ENSG00000167646	ENSG00000167646	HGNC:30492													
DNAAF4	gene	DNAAF4	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Ciliary dyskinesia, primary, 25, 615482 (3)						False	3	0;0;0	0.109	False		ENSG00000256061	ENSG00000256061	HGNC:21493													
DNAAF5	gene	DNAAF5	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Ciliary dyskinesia, primary, 18, 614874 (3)						False	3	0;0;0	0.109	False		ENSG00000164818	ENSG00000164818	HGNC:26013													
DNAH11	gene	DNAH11	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Ciliary dyskinesia, primary, 7, with or without situs inversus, 611884 (3)						False	3	0;0;0	0.109	False		ENSG00000105877	ENSG00000105877	HGNC:2942													
DNAH5	gene	DNAH5	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Ciliary dyskinesia, primary, 3, with or without situs inversus, 608644 (3)						False	3	0;0;0	0.109	False		ENSG00000039139	ENSG00000039139	HGNC:2950													
DNAI1	gene	DNAI1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Ciliary dyskinesia, primary, 1, with or without situs inversus, 244400 (3)						False	3	0;0;0	0.109	False		ENSG00000122735	ENSG00000122735	HGNC:2954													
DNAI2	gene	DNAI2	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Ciliary dyskinesia, primary, 9, with or without situs inversus, 612444 (3)						False	3	0;0;0	0.109	False		ENSG00000171595	ENSG00000171595	HGNC:18744													
DNAJC12	gene	DNAJC12	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Hyperphenylalaninemia, mild, non-BH4-deficient, 617384 (3), Autosomal recessive						False	3	0;0;0	0.109	False		ENSG00000108176	ENSG00000108176	HGNC:28908													
DNAJC19	gene	DNAJC19	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	3-methylglutaconic aciduria, type V, 610198 (3)						False	3	0;0;0	0.109	False		ENSG00000205981	ENSG00000205981	HGNC:30528													
DNAJC21	gene	DNAJC21	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Bone marrow failure syndrome 3, 617052 (3), Autosomal recessive						False	3	0;0;0	0.109	False		ENSG00000168724	ENSG00000168724	HGNC:27030													
DNAJC6	gene	DNAJC6	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Parkinson disease 19, juvenile-onset, 615528 (3)						False	3	0;0;0	0.109	False		ENSG00000116675	ENSG00000116675	HGNC:15469													
DNMT3B	gene	DNMT3B	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Immunodeficiency-centromeric instability-facial anomalies syndrome 1, 242860 (3)						False	3	0;0;0	0.109	False		ENSG00000088305	ENSG00000088305	HGNC:2979													
DOCK2	gene	DOCK2	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Immunodeficiency 40, 616433 (3)						False	3	0;0;0	0.109	False		ENSG00000134516	ENSG00000134516	HGNC:2988													
DOCK6	gene	DOCK6	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Adams-Oliver syndrome 2, 614219 (3)						False	3	0;0;0	0.109	False		ENSG00000130158	ENSG00000130158	HGNC:19189													
DOCK8	gene	DOCK8	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Hyper-IgE recurrent infection syndrome, autosomal recessive, 243700 (3)						False	3	0;0;0	0.109	False		ENSG00000107099	ENSG00000107099	HGNC:19191													
DOK7	gene	DOK7	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Myasthenic syndrome, congenital, 10, 254300 (3)						False	3	0;0;0	0.109	False		ENSG00000175920	ENSG00000175920	HGNC:26594													
DOLK	gene	DOLK	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Congenital disorder of glycosylation, type Im, 610768 (3)						False	3	0;0;0	0.109	False		ENSG00000175283	ENSG00000175283	HGNC:23406													
DONSON	gene	DONSON	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Microcephaly, short stature, and limb abnormalities, 617604 (3), Autosomal recessive						False	3	0;0;0	0.109	False		ENSG00000159147	ENSG00000159147	HGNC:2993													
DPAGT1	gene	DPAGT1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Myasthenic syndrome, congenital, 13, with tubular aggregates, 614750 (3)						False	3	100;0;0	0.109	False		ENSG00000172269	ENSG00000172269	HGNC:2995													
DPH1	gene	DPH1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Developmental delay with short stature, dysmorphic features, and sparse hair, 616901 (3), Autosomal recessive						False	3	0;0;0	0.109	False		ENSG00000108963	ENSG00000108963	HGNC:3003													
DSP	gene	DSP	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Cardiomyopathy, dilated, with woolly hair and keratoderma, 605676 (3)						False	3	0;0;0	0.109	False		ENSG00000096696	ENSG00000096696	HGNC:3052													
DSTYK	gene	DSTYK	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Spastic paraplegia 23, 270750 (3), Autosomal recessive						False	3	0;100;0	0.109	False		ENSG00000133059	ENSG00000133059	HGNC:29043													
DYM	gene	DYM	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Dyggve-Melchior-Clausen disease, 223800 (3)						False	3	0;0;0	0.109	False		ENSG00000141627	ENSG00000141627	HGNC:21317													
DYNC2H1	gene	DYNC2H1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Short-rib thoracic dysplasia 3 with or without polydactyly, 613091 (3)						False	3	0;0;0	0.109	False		ENSG00000187240	ENSG00000187240	HGNC:2962													
DYNC2LI1	gene	DYNC2LI1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Short-rib thoracic dysplasia 15 with polydactyly, 617088 (3), Autosomal recessive						False	3	0;0;0	0.109	False		ENSG00000138036	ENSG00000138036	HGNC:24595													
DYSF	gene	DYSF	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Muscular dystrophy, limb-girdle, type 2B, 253601 (3)						False	3	0;0;0	0.109	False		ENSG00000135636	ENSG00000135636	HGNC:3097													
EARS2	gene	EARS2	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Combined oxidative phosphorylation deficiency 12, 614924 (3)						False	3	0;0;0	0.109	False		ENSG00000103356	ENSG00000103356	HGNC:29419													
ECEL1	gene	ECEL1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Arthrogryposis, distal, type 5D, 615065 (3)						False	3	0;0;0	0.109	False		ENSG00000171551	ENSG00000171551	HGNC:3147													
ECHS1	gene	ECHS1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Mitochondrial short-chain enoyl-CoA hydratase 1 deficiency, 616277 (3)						False	3	0;0;0	0.109	False		ENSG00000127884	ENSG00000127884	HGNC:3151													
EDA	gene	EDA	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	X-LINKED: hemizygous mutation in males, biallelic mutations in females	Ectodermal dysplasia 1, hypohidrotic, X-linked, 305100 (3)						False	3	100;0;0	0.109	True		ENSG00000158813	ENSG00000158813	HGNC:3157													
EDAR	gene	EDAR	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Ectodermal dysplasia 10B, hypohidrotic/hair/tooth type, autosomal recessive, 224900 (3)						False	3	0;0;0	0.109	False		ENSG00000135960	ENSG00000135960	HGNC:2895													
EFEMP2	gene	EFEMP2	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Cutis laxa, autosomal recessive, type IB, 614437 (3)						False	3	0;0;0	0.109	False		ENSG00000172638	ENSG00000172638	HGNC:3219													
EFNB1	gene	EFNB1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	X-LINKED: hemizygous mutation in males, biallelic mutations in females	Craniofrontonasal dysplasia, 304110 (3)						False	3	0;0;0	0.109	False		ENSG00000090776	ENSG00000090776	HGNC:3226													
EIF2AK3	gene	EIF2AK3	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Wolcott-Rallison syndrome, 226980 (3)						False	3	0;0;0	0.109	False		ENSG00000172071	ENSG00000172071	HGNC:3255													
EIF2AK4	gene	EIF2AK4	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Pulmonary venoocclusive disease 2, 234810 (3)						False	3	0;0;0	0.109	False		ENSG00000128829	ENSG00000128829	HGNC:19687													
EIF2B1	gene	EIF2B1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Leukoencephalopathy with vanishing white matter, 603896 (3)						False	3	0;0;0	0.109	False		ENSG00000111361	ENSG00000111361	HGNC:3257													
EIF2B2	gene	EIF2B2	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Leukoencephalopathy with vanishing white matter, 603896 (3)						False	3	0;0;0	0.109	False		ENSG00000119718	ENSG00000119718	HGNC:3258													
EIF2B3	gene	EIF2B3	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Leukoencephalopathy with vanishing white matter, 603896 (3)						False	3	0;0;0	0.109	False		ENSG00000070785	ENSG00000070785	HGNC:3259													
EIF2B4	gene	EIF2B4	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Leukoencephaly with vanishing white matter, 603896 (3)						False	3	0;0;0	0.109	False		ENSG00000115211	ENSG00000115211	HGNC:3260													
EIF2B5	gene	EIF2B5	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Leukoencephalopathy with vanishing white matter, 603896 (3)						False	3	0;0;0	0.109	False		ENSG00000145191	ENSG00000145191	HGNC:3261													
EIF2S3	gene	EIF2S3	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	X-LINKED: hemizygous mutation in males, biallelic mutations in females	MEHMO syndrome, 300148 (3), X-linked recessive						False	3	0;0;0	0.109	False		ENSG00000130741	ENSG00000130741	HGNC:3267													
ELAC2	gene	ELAC2	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Combined oxidative phosphorylation deficiency 17, 615440 (3)						False	3	0;0;0	0.109	False		ENSG00000006744	ENSG00000006744	HGNC:14198													
ELP1	gene	ELP1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Dysautonomia, familial, 223900 (3)						False	3	0;0;0	0.109	False		ENSG00000070061	ENSG00000070061	HGNC:5959													
ELP2	gene	ELP2	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Mental retardation, autosomal recessive 58, 617270 (3)						False	3	0;0;0	0.109	False		ENSG00000134759	ENSG00000134759	HGNC:18248													
EMD	gene	EMD	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	X-LINKED: hemizygous mutation in males, biallelic mutations in females	Emery-Dreifuss muscular dystrophy 1, X-linked, 310300 (3)						False	3	0;0;0	0.109	False		ENSG00000102119	ENSG00000102119	HGNC:3331													
EMG1	gene	EMG1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Bowen-Conradi syndrome, 211180 (3)						False	3	100;0;0	0.109	False		ENSG00000126749	ENSG00000126749	HGNC:16912													
EML1	gene	EML1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Band heterotopia, 600348 (3), Autosomal recessive						False	3	0;0;0	0.109	False		ENSG00000066629	ENSG00000066629	HGNC:3330													
ENPP1	gene	ENPP1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Hypophosphatemic rickets, autosomal recessive, 2, 613312 (3)						False	3	0;0;0	0.109	False		ENSG00000197594	ENSG00000197594	HGNC:3356													
EOGT	gene	EOGT	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Adams-Oliver syndrome 4, 615297 (3)						False	3	0;0;0	0.109	False		ENSG00000163378	ENSG00000163378	HGNC:28526													
EPCAM	gene	EPCAM	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Diarrhea 5, with tufting enteropathy, congenital, 613217 (3)						False	3	0;0;0	0.109	False		ENSG00000119888	ENSG00000119888	HGNC:11529													
EPG5	gene	EPG5	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Vici syndrome, 242840 (3)						False	3	0;0;0	0.109	False		ENSG00000152223	ENSG00000152223	HGNC:29331													
EPM2A	gene	EPM2A	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Epilepsy, progressive myoclonic 2A (Lafora), 254780 (3)						False	3	0;0;0	0.109	False		ENSG00000112425	ENSG00000112425	HGNC:3413													
ERCC2	gene	ERCC2	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Cerebrooculofacioskeletal syndrome 2, 610756 (3)						False	3	0;0;0	0.109	False		ENSG00000104884	ENSG00000104884	HGNC:3434													
ERCC4	gene	ERCC4	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Fanconi anemia, complementation group Q, 615272 (3)						False	3	0;0;0	0.109	False		ENSG00000175595	ENSG00000175595	HGNC:3436													
ERCC5	gene	ERCC5	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Xeroderma pigmentosum, group G, 278780 (3)						False	3	0;0;0	0.109	False		ENSG00000134899	ENSG00000134899	HGNC:3437													
ERCC6	gene	ERCC6	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Cockayne syndrome, type B, 133540 (3)						False	3	0;0;0	0.109	False		ENSG00000225830	ENSG00000225830	HGNC:3438													
ERCC6L2	gene	ERCC6L2	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Bone marrow failure syndrome 2, 615715 (3)						False	3	0;0;0	0.109	False		ENSG00000182150	ENSG00000182150	HGNC:26922													
ERCC8	gene	ERCC8	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Cockayne syndrome, type A, 216400 (3)						False	3	0;0;0	0.109	False		ENSG00000049167	ENSG00000049167	HGNC:3439													
ESCO2	gene	ESCO2	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	SC phocomelia syndrome, 269000 (3)						False	3	0;0;0	0.109	False		ENSG00000171320	ENSG00000171320	HGNC:27230													
ETFA	gene	ETFA	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Glutaric acidemia IIA, 231680 (3)						False	3	0;0;0	0.109	False		ENSG00000140374	ENSG00000140374	HGNC:3481													
ETFB	gene	ETFB	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Glutaric acidemia IIB, 231680 (3)						False	3	0;0;0	0.109	False		ENSG00000105379	ENSG00000105379	HGNC:3482													
ETFDH	gene	ETFDH	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Glutaric acidemia IIC, 231680 (3)						False	3	0;0;0	0.109	False		ENSG00000171503	ENSG00000171503	HGNC:3483													
ETHE1	gene	ETHE1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Ethylmalonic encephalopathy, 602473 (3)						False	3	0;0;0	0.109	False		ENSG00000105755	ENSG00000105755	HGNC:23287													
EVC	gene	EVC	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Ellis-van Creveld syndrome, 225500 (3)						False	3	0;0;0	0.109	False		ENSG00000072840	ENSG00000072840	HGNC:3497													
EVC2	gene	EVC2	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Ellis-van Creveld syndrome, 225500 (3)						False	3	0;0;0	0.109	False		ENSG00000173040	ENSG00000173040	HGNC:19747													
EXOSC3	gene	EXOSC3	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Pontocerebellar hypoplasia, type 1B, 614678 (3)						False	3	0;0;0	0.109	False		ENSG00000107371	ENSG00000107371	HGNC:17944													
EXOSC8	gene	EXOSC8	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Pontocerebellar hypoplasia, type 1C, 616081 (3)						False	3	0;0;0	0.109	False		ENSG00000120699	ENSG00000120699	HGNC:17035													
EXTL3	gene	EXTL3	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Immunoskeletal dysplasia with neurodevelopmental abnormalities, 617425 (3), Autosomal recessive						False	3	0;0;0	0.109	False		ENSG00000012232	ENSG00000012232	HGNC:3518													
F2	gene	F2	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Dysprothrombinemia, 613679 (3)						False	3	0;0;0	0.109	False		ENSG00000180210	ENSG00000180210	HGNC:3535													
F5	gene	F5	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Factor V deficiency, 227400 (3)						False	3	0;0;0	0.109	False		ENSG00000198734	ENSG00000198734	HGNC:3542													
F7	gene	F7	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Factor VII deficiency, 227500 (3)						False	3	0;0;0	0.109	False		ENSG00000057593	ENSG00000057593	HGNC:3544													
F8	gene	F8	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	X-LINKED: hemizygous mutation in males, biallelic mutations in females	Hemophilia A, 306700 (3)						False	3	0;0;0	0.109	False		ENSG00000185010	ENSG00000185010	HGNC:3546													
F9	gene	F9	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	X-LINKED: hemizygous mutation in males, biallelic mutations in females	Hemophilia B, 306900 (3)						False	3	0;0;0	0.109	False		ENSG00000101981	ENSG00000101981	HGNC:3551													
FA2H	gene	FA2H	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Spastic paraplegia 35, autosomal recessive, 612319 (3)						False	3	0;0;0	0.109	False		ENSG00000103089	ENSG00000103089	HGNC:21197													
FAH	gene	FAH	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Tyrosinemia, type I, 276700 (3)						False	3	0;0;0	0.109	False		ENSG00000103876	ENSG00000103876	HGNC:3579													
FAM126A	gene	FAM126A	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Leukodystrophy, hypomyelinating, 5, 610532 (3)						False	3	0;0;0	0.109	False		ENSG00000122591	ENSG00000122591	HGNC:24587													
FAM20C	gene	FAM20C	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Raine syndrome, 259775 (3)						False	3	0;0;0	0.109	False		ENSG00000177706	ENSG00000177706	HGNC:22140													
FANCA	gene	FANCA	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Fanconi anemia, complementation group A, 227650 (3)						False	3	0;0;0	0.109	False		ENSG00000187741	ENSG00000187741	HGNC:3582													
FANCB	gene	FANCB	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	X-LINKED: hemizygous mutation in males, biallelic mutations in females	Fanconi anemia, complementation group B, 300514 (3)						False	3	0;0;0	0.109	False		ENSG00000181544	ENSG00000181544	HGNC:3583													
FANCC	gene	FANCC	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Fanconi anemia, complementation group C, 227645 (3)						False	3	0;0;0	0.109	False		ENSG00000158169	ENSG00000158169	HGNC:3584													
FANCD2	gene	FANCD2	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Fanconi anemia, complementation group D2, 227646 (3)						False	3	0;0;0	0.109	False		ENSG00000144554	ENSG00000144554	HGNC:3585													
FANCE	gene	FANCE	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Fanconi anemia, complementation group E, 600901 (3)						False	3	0;0;0	0.109	False		ENSG00000112039	ENSG00000112039	HGNC:3586													
FANCF	gene	FANCF	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Fanconi anemia, complementation group F, 603467 (3)						False	3	0;0;0	0.109	False		ENSG00000183161	ENSG00000183161	HGNC:3587													
FANCG	gene	FANCG	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Fanconi anemia, complementation group G, 614082 (3)						False	3	0;0;0	0.109	False		ENSG00000221829	ENSG00000221829	HGNC:3588													
FANCI	gene	FANCI	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Fanconi anemia, complementation group I, 609053 (3)						False	3	0;0;0	0.109	False		ENSG00000140525	ENSG00000140525	HGNC:25568													
FANCL	gene	FANCL	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Fanconi anemia, complementation group L, 614083 (3)						False	3	0;0;0	0.109	False		ENSG00000115392	ENSG00000115392	HGNC:20748													
FARS2	gene	FARS2	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Combined oxidative phosphorylation deficiency 14, 614946 (3)						False	3	0;0;0	0.109	False		ENSG00000145982	ENSG00000145982	HGNC:21062													
FAT4	gene	FAT4	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Hennekam lymphangiectasia-lymphedema syndrome 2, 616006 (3)						False	3	0;0;0	0.109	False		ENSG00000196159	ENSG00000196159	HGNC:23109													
FBLN5	gene	FBLN5	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Cutis laxa, autosomal recessive, type IA, 219100 (3)						False	3	0;0;0	0.109	False		ENSG00000140092	ENSG00000140092	HGNC:3602													
FBP1	gene	FBP1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Fructose-1,6-bisphosphatase deficiency, 229700 (3)						False	3	0;0;0	0.109	False		ENSG00000165140	ENSG00000165140	HGNC:3606													
FBXL4	gene	FBXL4	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Mitochondrial DNA depletion syndrome 13 (encephalomyopathic type), 615471 (3)						False	3	0;0;0	0.109	False		ENSG00000112234	ENSG00000112234	HGNC:13601													
FBXO7	gene	FBXO7	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Parkinson disease 15, autosomal recessive, 260300 (3)						False	3	0;0;0	0.109	False		ENSG00000100225	ENSG00000100225	HGNC:13586													
FERMT1	gene	FERMT1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Kindler syndrome, 173650 (3)						False	3	0;0;0	0.109	False		ENSG00000101311	ENSG00000101311	HGNC:15889													
FERMT3	gene	FERMT3	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Leukocyte adhesion deficiency, type III, 612840 (3)						False	3	0;0;0	0.109	False		ENSG00000149781	ENSG00000149781	HGNC:23151													
FGA	gene	FGA	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Afibrinogenemia, congenital, 202400 (3)						False	3	0;0;0	0.109	False		ENSG00000171560	ENSG00000171560	HGNC:3661													
FGB	gene	FGB	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Afibrinogenemia, congenital, 202400 (3)						False	3	0;0;0	0.109	False		ENSG00000171564	ENSG00000171564	HGNC:3662													
FGD4	gene	FGD4	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Charcot-Marie-Tooth disease, type 4H, 609311 (3)						False	3	0;0;0	0.109	False		ENSG00000139132	ENSG00000139132	HGNC:19125													
FGG	gene	FGG	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Afibrinogenemia, congenital, 202400 (3)						False	3	0;0;0	0.109	False		ENSG00000171557	ENSG00000171557	HGNC:3694													
FH	gene	FH	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Fumarase deficiency, 606812 (3)						False	3	0;0;0	0.109	False		ENSG00000091483	ENSG00000091483	HGNC:3700													
FHL1	gene	FHL1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	X-LINKED: hemizygous mutation in males, biallelic mutations in females	Emery-Dreifuss muscular dystrophy 6, X-linked, 300696 (3)						False	3	0;0;0	0.109	False		ENSG00000022267	ENSG00000022267	HGNC:3702													
FIG4	gene	FIG4	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Yunis-Varon syndrome, 216340 (3)						False	3	0;0;0	0.109	False		ENSG00000112367	ENSG00000112367	HGNC:16873													
FKBP10	gene	FKBP10	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Bruck syndrome 1, 259450 (3)						False	3	0;0;0	0.109	False		ENSG00000141756	ENSG00000141756	HGNC:18169													
FKBP14	gene	FKBP14	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Ehlers-Danlos syndrome with progressive kyphoscoliosis, myopathy, and hearing loss, 614557 (3)						False	3	0;0;0	0.109	False		ENSG00000106080	ENSG00000106080	HGNC:18625													
FKRP	gene	FKRP	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 5, 613153 (3)						False	3	0;0;0	0.109	False		ENSG00000181027	ENSG00000181027	HGNC:17997													
FKTN	gene	FKTN	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 4, 253800 (3)						False	3	0;0;0	0.109	False		ENSG00000106692	ENSG00000106692	HGNC:3622													
FLAD1	gene	FLAD1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Lipid storage myopathy due to flavin adenine dinucleotide synthetase deficiency, 255100 (3), Autosomal recessive						False	3	0;0;0	0.109	False		ENSG00000160688	ENSG00000160688	HGNC:24671													
FLNA	gene	FLNA	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	X-LINKED: hemizygous mutation in males, biallelic mutations in females	FG syndrome 2, 300321 (3)						False	3	0;0;0	0.109	False		ENSG00000196924	ENSG00000196924	HGNC:3754													
FLNB	gene	FLNB	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Spondylocarpotarsal synostosis syndrome, 272460 (3)						False	3	0;0;0	0.109	False		ENSG00000136068	ENSG00000136068	HGNC:3755													
FLVCR1	gene	FLVCR1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Ataxia, posterior column, with retinitis pigmentosa, 609033 (3)						False	3	0;0;0	0.109	False		ENSG00000162769	ENSG00000162769	HGNC:24682													
FLVCR2	gene	FLVCR2	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Proliferative vasculopathy and hydraencephaly-hydrocephaly syndrome, 225790 (3)						False	3	0;0;0	0.109	False		ENSG00000119686	ENSG00000119686	HGNC:20105													
FMR1	gene	FMR1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	X-LINKED: hemizygous mutation in males, biallelic mutations in females	Fragile X syndrome						False	3	0;0;0	0.109	False		ENSG00000102081	ENSG00000102081	HGNC:3775													
FOLR1	gene	FOLR1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Neurodegeneration due to cerebral folate transport deficiency, 613068 (3)						False	3	0;0;0	0.109	False		ENSG00000110195	ENSG00000110195	HGNC:3791													
FOXE3	gene	FOXE3	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Aphakia, congenital primary, 610256 (3)						False	3	0;0;0	0.109	False		ENSG00000186790	ENSG00000186790	HGNC:3808													
FOXN1	gene	FOXN1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	T-cell immunodeficiency, congenital alopecia, and nail dystrophy, 601705 (3)						False	3	0;0;0	0.109	False		ENSG00000109101	ENSG00000109101	HGNC:12765													
FOXP3	gene	FOXP3	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	X-LINKED: hemizygous mutation in males, biallelic mutations in females	Immunodysregulation, polyendocrinopathy, and enteropathy, X-linked, 304790 (3)						False	3	0;0;0	0.109	False		ENSG00000049768	ENSG00000049768	HGNC:6106													
FOXRED1	gene	FOXRED1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Mitochondrial complex I deficiency, 252010 (3)						False	3	0;0;0	0.109	False		ENSG00000110074	ENSG00000110074	HGNC:26927													
FRAS1	gene	FRAS1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Fraser syndrome, 219000 (3)						False	3	0;0;0	0.109	False		ENSG00000138759	ENSG00000138759	HGNC:19185													
FREM1	gene	FREM1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Bifid nose with or without anorectal and renal anomalies, 608980 (3)						False	3	0;0;0	0.109	False		ENSG00000164946	ENSG00000164946	HGNC:23399													
FREM2	gene	FREM2	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Fraser syndrome, 219000 (3)						False	3	0;0;0	0.109	False		ENSG00000150893	ENSG00000150893	HGNC:25396													
FRRS1L	gene	FRRS1L	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Epileptic encephalopathy, early infantile, 37, 616981 (3), Autosomal recessive						False	3	0;0;0	0.109	False		ENSG00000260230	ENSG00000260230	HGNC:1362													
FTCD	gene	FTCD	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Glutamate formiminotransferase deficiency, 229100 (3)						False	3	0;0;100	0.109	False		ENSG00000160282	ENSG00000160282	HGNC:3974													
FTO	gene	FTO	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Growth retardation, developmental delay, coarse facies, and early death, 612938 (3)						False	3	0;0;0	0.109	False		ENSG00000140718	ENSG00000140718	HGNC:24678													
FTSJ1	gene	FTSJ1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	X-LINKED: hemizygous mutation in males, biallelic mutations in females	Mental retardation, X-linked 9, 309549 (3)						False	3	0;0;0	0.109	False		ENSG00000068438	ENSG00000068438	HGNC:13254													
FUCA1	gene	FUCA1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Fucosidosis, 230000 (3)						False	3	0;0;0	0.109	False		ENSG00000179163	ENSG00000179163	HGNC:4006													
FYCO1	gene	FYCO1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Cataract 18, autosomal recessive, 610019 (3)						False	3	0;0;0	0.109	False		ENSG00000163820	ENSG00000163820	HGNC:14673													
G6PC	gene	G6PC	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Glycogen storage disease Ia, 232200 (3)						False	3	0;0;0	0.109	False		ENSG00000131482	ENSG00000131482	HGNC:4056													
G6PC3	gene	G6PC3	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Dursun syndrome, 612541 (3)						False	3	0;0;0	0.109	False		ENSG00000141349	ENSG00000141349	HGNC:24861													
GAA	gene	GAA	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Glycogen storage disease II, 232300 (3)						False	3	0;0;0	0.109	False		ENSG00000171298	ENSG00000171298	HGNC:4065													
GALC	gene	GALC	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Krabbe disease, 245200 (3)						False	3	0;0;0	0.109	False		ENSG00000054983	ENSG00000054983	HGNC:4115													
GALNS	gene	GALNS	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Mucopolysaccharidosis IVA, 253000 (3)						False	3	0;0;0	0.109	False		ENSG00000141012	ENSG00000141012	HGNC:4122													
GALT	gene	GALT	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Galactosemia, 230400 (3)						False	3	100;0;0	0.109	True		ENSG00000213930	ENSG00000213930	HGNC:4135													
GAMT	gene	GAMT	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Cerebral creatine deficiency syndrome 2, 612736 (3)						False	3	0;0;0	0.109	False		ENSG00000130005	ENSG00000130005	HGNC:4136													
GAN	gene	GAN	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Giant axonal neuropathy-1, 256850 (3)						False	3	0;0;0	0.109	False		ENSG00000261609	ENSG00000261609	HGNC:4137													
GAS8	gene	GAS8	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Ciliary dyskinesia, primary, 33, 616726 (3), Autosomal recessive						False	3	0;0;0	0.109	False		ENSG00000141013	ENSG00000141013	HGNC:4166													
GATM	gene	GATM	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Cerebral creatine deficiency syndrome 3, 612718 (3)						False	3	0;0;0	0.109	False		ENSG00000171766	ENSG00000171766	HGNC:4175													
GBA	gene	GBA	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Gaucher disease, perinatal lethal, 608013 (3)						False	3	0;0;0	0.109	False		ENSG00000177628	ENSG00000177628	HGNC:4177													
GBA2	gene	GBA2	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Spastic paraplegia 46, autosomal recessive, 614409 (3)						False	3	0;0;0	0.109	False		ENSG00000070610	ENSG00000070610	HGNC:18986													
GBE1	gene	GBE1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Glycogen storage disease IV, 232500 (3)						False	3	0;0;0	0.109	False		ENSG00000114480	ENSG00000114480	HGNC:4180													
GCDH	gene	GCDH	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Glutaricaciduria, type I, 231670 (3)						False	3	0;0;0	0.109	False		ENSG00000105607	ENSG00000105607	HGNC:4189													
GCH1	gene	GCH1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Dystonia, DOPA-responsive, with or without hyperphenylalaninemia, 128230 (3)						False	3	0;0;0	0.109	False		ENSG00000131979	ENSG00000131979	HGNC:4193													
GDAP1	gene	GDAP1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Charcot-Marie-Tooth disease, recessive intermediate, A, 608340 (3)						False	3	0;0;0	0.109	False		ENSG00000104381	ENSG00000104381	HGNC:15968													
GDF1	gene	GDF1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Right atrial isomerism, 208530 (3)						False	3	0;0;0	0.109	False		ENSG00000130283	ENSG00000130283	HGNC:4214													
GDF5	gene	GDF5	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Chondrodysplasia, Grebe type, 200700 (3)						False	3	0;0;0	0.109	False		ENSG00000125965	ENSG00000125965	HGNC:4220													
GDI1	gene	GDI1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	X-LINKED: hemizygous mutation in males, biallelic mutations in females	Mental retardation, X-linked 41, 300849 (3)						False	3	0;0;0	0.109	False		ENSG00000203879	ENSG00000203879	HGNC:4226													
GFM1	gene	GFM1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Combined oxidative phosphorylation deficiency 1, 609060 (3)						False	3	0;0;0	0.109	False		ENSG00000168827	ENSG00000168827	HGNC:13780													
GFPT1	gene	GFPT1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Myasthenia, congenital, 12, with tubular aggregates, 610542 (3)						False	3	0;0;0	0.109	False		ENSG00000198380	ENSG00000198380	HGNC:4241													
GHR	gene	GHR	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Laron dwarfism, 262500 (3)						False	3	0;0;0	0.109	False		ENSG00000112964	ENSG00000112964	HGNC:4263													
GJA1	gene	GJA1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Hypoplastic left heart syndrome 1, 241550 (3)						False	3	0;0;0	0.109	False		ENSG00000152661	ENSG00000152661	HGNC:4274													
GJC2	gene	GJC2	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Leukodystrophy, hypomyelinating, 2, 608804 (3)						False	3	0;0;0	0.109	False		ENSG00000198835	ENSG00000198835	HGNC:17494													
GK	gene	GK	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	X-LINKED: hemizygous mutation in males, biallelic mutations in females	Glycerol kinase deficiency, 307030 (3)						False	3	0;0;100	0.109	False		ENSG00000198814	ENSG00000198814	HGNC:4289													
GLA	gene	GLA	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	X-LINKED: hemizygous mutation in males, biallelic mutations in females	Fabry disease, 301500 (3)						False	3	0;0;0	0.109	False		ENSG00000102393	ENSG00000102393	HGNC:4296													
GLB1	gene	GLB1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Mucopolysaccharidosis type IVB (Morquio), 253010 (3)						False	3	0;0;0	0.109	False		ENSG00000170266	ENSG00000170266	HGNC:4298													
GLDC	gene	GLDC	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Glycine encephalopathy, 605899 (3)						False	3	0;0;0	0.109	False		ENSG00000178445	ENSG00000178445	HGNC:4313													
GLDN	gene	GLDN	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Lethal congenital contracture syndrome 11, 617194 (3), Autosomal recessive						False	3	0;0;0	0.109	False		ENSG00000186417	ENSG00000186417	HGNC:29514													
GLE1	gene	GLE1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Arthrogryposis, lethal, with anterior horn cell disease, 611890 (3)						False	3	0;0;0	0.109	False		ENSG00000119392	ENSG00000119392	HGNC:4315													
GLIS3	gene	GLIS3	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Diabetes mellitus, neonatal, with congenital hypothyroidism, 610199 (3)						False	3	0;0;0	0.109	False		ENSG00000107249	ENSG00000107249	HGNC:28510													
GLYCTK	gene	GLYCTK	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	D-glyceric aciduria, 220120 (3)						False	3	0;0;0	0.109	False		ENSG00000168237	ENSG00000168237	HGNC:24247													
GM2A	gene	GM2A	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	GM2-gangliosidosis, AB variant, 272750 (3)						False	3	0;0;0	0.109	False		ENSG00000196743	ENSG00000196743	HGNC:4367													
GMPPA	gene	GMPPA	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Alacrima, achalasia, and mental retardation syndrome, 615510 (3)						False	3	0;0;0	0.109	False		ENSG00000144591	ENSG00000144591	HGNC:22923													
GMPPB	gene	GMPPB	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 14, 615352 (3)						False	3	0;0;0	0.109	False		ENSG00000173540	ENSG00000173540	HGNC:22932													
GNAT2	gene	GNAT2	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Achromatopsia-4, 613856 (3)						False	3	0;0;0	0.109	False		ENSG00000134183	ENSG00000134183	HGNC:4394													
GNB5	gene	GNB5	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Intellectual developmental disorder with cardiac arrhythmia, 617173 (3), Autosomal recessive						False	3	0;0;0	0.109	False		ENSG00000069966	ENSG00000069966	HGNC:4401													
GNE	gene	GNE	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Inclusion body myopathy, autosomal recessive, 600737 (3)						False	3	0;0;0	0.109	False		ENSG00000159921	ENSG00000159921	HGNC:23657													
GNPAT	gene	GNPAT	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Chondrodysplasia punctata, rhizomelic, type 2, 222765 (3)						False	3	0;0;0	0.109	False		ENSG00000116906	ENSG00000116906	HGNC:4416													
GNPTAB	gene	GNPTAB	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Mucolipidosis III alpha/beta, 252600 (3)						False	3	0;0;0	0.109	False		ENSG00000111670	ENSG00000111670	HGNC:29670													
GNPTG	gene	GNPTG	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Mucolipidosis III gamma, 252605 (3)						False	3	0;0;0	0.109	False		ENSG00000090581	ENSG00000090581	HGNC:23026													
GNS	gene	GNS	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Mucopolysaccharidosis type IIID, 252940 (3)						False	3	0;0;0	0.109	False		ENSG00000135677	ENSG00000135677	HGNC:4422													
GORAB	gene	GORAB	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Geroderma osteodysplasticum, 231070 (3)						False	3	0;0;0	0.109	False		ENSG00000120370	ENSG00000120370	HGNC:25676													
GOSR2	gene	GOSR2	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Epilepsy, progressive myoclonic 6, 614018 (3)						False	3	0;0;0	0.109	False		ENSG00000108433	ENSG00000108433	HGNC:4431													
GPAA1	gene	GPAA1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Glycosylphosphatidylinositol biosynthesis defect 15, 617810 (3), Autosomal recessive						False	3	0;0;0	0.109	False		ENSG00000197858	ENSG00000197858	HGNC:4446													
GPC3	gene	GPC3	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	X-LINKED: hemizygous mutation in males, biallelic mutations in females	Simpson-Golabi-Behmel syndrome, type 1, 312870 (3)						False	3	0;0;0	0.109	False		ENSG00000147257	ENSG00000147257	HGNC:4451													
GPC6	gene	GPC6	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Omodysplasia 1, 258315 (3)						False	3	0;0;0	0.109	False		ENSG00000183098	ENSG00000183098	HGNC:4454													
GPHN	gene	GPHN	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Molybdenum cofactor deficiency C, 615501 (3)						False	3	0;0;0	0.109	False		ENSG00000171723	ENSG00000171723	HGNC:15465													
GPR143	gene	GPR143	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	X-LINKED: hemizygous mutation in males, biallelic mutations in females	Ocular albinism, type I, Nettleship-Falls type, 300500 (3)						False	3	0;0;0	0.109	False		ENSG00000101850	ENSG00000101850	HGNC:20145													
GPR179	gene	GPR179	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Night blindness, congenital stationary (complete), 1E, autosomal recessive, 614565 (3)						False	3	0;0;0	0.109	False		ENSG00000188888	ENSG00000277399	HGNC:31371													
GPSM2	gene	GPSM2	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Chudley-McCullough syndrome, 604213 (3)						False	3	0;0;0	0.109	False		ENSG00000121957	ENSG00000121957	HGNC:29501													
GPT2	gene	GPT2	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Mental retardation, autosomal recessive 49, 616281 (3)						False	3	0;0;0	0.109	False		ENSG00000166123	ENSG00000166123	HGNC:18062													
GRM1	gene	GRM1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Spinocerebellar ataxia, autosomal recessive 13, 614831 (3)						False	3	0;0;0	0.109	False		ENSG00000152822	ENSG00000152822	HGNC:4593													
GSS	gene	GSS	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Glutathione synthetase deficiency, 266130 (3)						False	3	0;0;0	0.109	False		ENSG00000100983	ENSG00000100983	HGNC:4624													
GTF2H5	gene	GTF2H5	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Trichothiodystrophy 3, photosensitive, 616395 (3)						False	3	0;0;0	0.109	False		ENSG00000272047	ENSG00000272047	HGNC:21157													
GTPBP3	gene	GTPBP3	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Combined oxidative phosphorylation deficiency 23, 616198 (3)						False	3	0;0;0	0.109	False		ENSG00000130299	ENSG00000130299	HGNC:14880													
GUCY1A3	gene	GUCY1A3	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Moyamoya 6 with achalasia, 615750 (3)						False	3	0;0;0	0.109	False		ENSG00000164116	ENSG00000164116	HGNC:4685													
GUCY2C	gene	GUCY2C	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Meconium ileus, 614665 (3)						False	3	0;0;0	0.109	False		ENSG00000070019	ENSG00000070019	HGNC:4688													
GUCY2D	gene	GUCY2D	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Leber congenital amaurosis 1, 204000 (3)						False	3	0;0;0	0.109	False		ENSG00000132518	ENSG00000132518	HGNC:4689													
GUSB	gene	GUSB	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Mucopolysaccharidosis VII, 253220 (3)						False	3	0;0;0	0.109	False		ENSG00000169919	ENSG00000169919	HGNC:4696													
GYS2	gene	GYS2	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Glycogen storage disease 0, liver, 240600 (3)						False	3	0;0;0	0.109	False		ENSG00000111713	ENSG00000111713	HGNC:4707													
HACE1	gene	HACE1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Spastic paraplegia and psychomotor retardation with or without seizures, 616756 (3), Autosomal recessive						False	3	0;0;0	0.109	False		ENSG00000085382	ENSG00000085382	HGNC:21033													
HADH	gene	HADH	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	3-hydroxyacyl-CoA dehydrogenase deficiency, 231530 (3)						False	3	0;0;0	0.109	False		ENSG00000138796	ENSG00000138796	HGNC:4799													
HADHA	gene	HADHA	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Fatty liver, acute, of pregnancy, 609016 (3)						False	3	0;0;0	0.109	False		ENSG00000084754	ENSG00000084754	HGNC:4801													
HADHB	gene	HADHB	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Trifunctional protein deficiency, 609015 (3)						False	3	0;0;0	0.109	False		ENSG00000138029	ENSG00000138029	HGNC:4803													
HAMP	gene	HAMP	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Hemochromatosis, type 2B, 613313 (3)						False	3	0;0;0	0.109	False		ENSG00000105697	ENSG00000105697	HGNC:15598													
HAX1	gene	HAX1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Neutropenia, severe congenital 3, autosomal recessive, 610738 (3)						False	3	0;0;0	0.109	False		ENSG00000143575	ENSG00000143575	HGNC:16915													
HBB	gene	HBB	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Thalassemias, beta-, 613985 (3)						False	3	0;0;0	0.109	False		ENSG00000244734	ENSG00000244734	HGNC:4827													
HCFC1	gene	HCFC1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	X-LINKED: hemizygous mutation in males, biallelic mutations in females	Mental retardation, X-linked 3 (methylmalonic acidemia and homocysteinemia, cblX type ), 309541 (3)						False	3	0;0;0	0.109	False		ENSG00000172534	ENSG00000172534	HGNC:4839													
HEPACAM	gene	HEPACAM	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Megalencephalic leukoencephalopathy with subcortical cysts 2A, 613925 (3)						False	3	0;0;0	0.109	False		ENSG00000165478	ENSG00000165478	HGNC:26361													
HERC2	gene	HERC2	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Mental retardation, autosomal recessive 38, 615516 (3)						False	3	0;0;0	0.109	False		ENSG00000128731	ENSG00000128731	HGNC:4868													
HES7	gene	HES7	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Spondylocostal dysostosis 4, autosomal recessive, 613686 (3)						False	3	0;0;0	0.109	False		ENSG00000179111	ENSG00000179111	HGNC:15977													
HESX1	gene	HESX1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Septooptic dysplasia, 182230 (3)						False	3	0;0;0	0.109	False		ENSG00000163666	ENSG00000163666	HGNC:4877													
HEXA	gene	HEXA	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Tay-Sachs disease, 272800 (3)						False	3	0;0;0	0.109	False		ENSG00000213614	ENSG00000213614	HGNC:4878													
HEXB	gene	HEXB	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Sandhoff disease, infantile, juvenile, and adult forms, 268800 (3)						False	3	0;0;0	0.109	False		ENSG00000049860	ENSG00000049860	HGNC:4879													
HFE2	gene	HFE2	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Hemochromatosis, type 2A, 602390 (3)						False	3	0;0;0	0.109	True		ENSG00000168509	ENSG00000168509	HGNC:4887													
HGSNAT	gene	HGSNAT	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Mucopolysaccharidosis type IIIC (Sanfilippo C), 252930 (3)						False	3	0;0;0	0.109	False		ENSG00000165102	ENSG00000165102	HGNC:26527													
HIBCH	gene	HIBCH	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	3-hydroxyisobutryl-CoA hydrolase deficiency, 250620 (3)						False	3	0;0;0	0.109	False		ENSG00000198130	ENSG00000198130	HGNC:4908													
HINT1	gene	HINT1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Neuromyotonia and axonal neuropathy, autosomal recessive, 137200 (3)						False	3	0;0;0	0.109	False		ENSG00000169567	ENSG00000169567	HGNC:4912													
HK1	gene	HK1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Neuropathy, hereditary motor and sensory, Russe type, 605285 (3)						False	3	0;100;0	0.109	False		ENSG00000156515	ENSG00000156515	HGNC:4922													
HLCS	gene	HLCS	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Holocarboxylase synthetase deficiency, 253270 (3)						False	3	0;0;0	0.109	False		ENSG00000159267	ENSG00000159267	HGNC:4976													
HMGCL	gene	HMGCL	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	HMG-CoA lyase deficiency, 246450 (3)						False	3	0;0;0	0.109	False		ENSG00000117305	ENSG00000117305	HGNC:5005													
HMGCS2	gene	HMGCS2	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	HMG-CoA synthase-2 deficiency, 605911 (3)						False	3	0;0;0	0.109	False		ENSG00000134240	ENSG00000134240	HGNC:5008													
HOXA1	gene	HOXA1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Athabaskan brainstem dysgenesis syndrome, 601536 (3)						False	3	0;0;0	0.109	False		ENSG00000105991	ENSG00000105991	HGNC:5099													
HPD	gene	HPD	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Tyrosinemia, type III, 276710 (3)						False	3	100;0;0	0.109	False		ENSG00000158104	ENSG00000158104	HGNC:5147													
HPGD	gene	HPGD	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Cranioosteoarthropathy, 259100 (3)						False	3	0;0;0	0.109	False		ENSG00000164120	ENSG00000164120	HGNC:5154													
HPRT1	gene	HPRT1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	X-LINKED: hemizygous mutation in males, biallelic mutations in females	Lesch-Nyhan syndrome, 300322 (3)						False	3	0;0;0	0.109	False		ENSG00000165704	ENSG00000165704	HGNC:5157													
HPS1	gene	HPS1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Hermansky-Pudlak syndrome 1, 203300 (3)						False	3	0;0;0	0.109	False		ENSG00000107521	ENSG00000107521	HGNC:5163													
HPS3	gene	HPS3	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Hermansky-Pudlak syndrome 3, 614072 (3)						False	3	0;0;0	0.109	False		ENSG00000163755	ENSG00000163755	HGNC:15597													
HPS4	gene	HPS4	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Hermansky-Pudlak syndrome 4, 614073 (3)						False	3	0;0;0	0.109	False		ENSG00000100099	ENSG00000100099	HGNC:15844													
HPS5	gene	HPS5	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Hermansky-Pudlak syndrome 5, 614074 (3)						False	3	0;0;0	0.109	False		ENSG00000110756	ENSG00000110756	HGNC:17022													
HPS6	gene	HPS6	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Hermansky-Pudlak syndrome 6, 614075 (3)						False	3	0;0;0	0.109	False		ENSG00000166189	ENSG00000166189	HGNC:18817													
HPSE2	gene	HPSE2	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Urofacial syndrome 1, 236730 (3)						False	3	0;0;0	0.109	False		ENSG00000172987	ENSG00000172987	HGNC:18374													
HSD17B10	gene	HSD17B10	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	X-LINKED: hemizygous mutation in males, biallelic mutations in females	HSD10 mitochondrial disease						False	3	0;0;0	0.109	False		ENSG00000072506	ENSG00000072506	HGNC:4800													
HSD17B4	gene	HSD17B4	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	D-bifunctional protein deficiency, 261515 (3)						False	3	0;0;0	0.109	False		ENSG00000133835	ENSG00000133835	HGNC:5213													
HSD3B2	gene	HSD3B2	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	3-beta-hydroxysteroid dehydrogenase, type II, deficiency, 201810 (3)						False	3	0;0;0	0.109	False		ENSG00000203859	ENSG00000203859	HGNC:5218													
HSD3B7	gene	HSD3B7	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Bile acid synthesis defect, congenital, 1, 607765 (3)						False	3	0;0;0	0.109	False		ENSG00000099377	ENSG00000099377	HGNC:18324													
HSPD1	gene	HSPD1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Leukodystrophy, hypomyelinating, 4, 612233 (3)						False	3	0;0;0	0.109	False		ENSG00000144381	ENSG00000144381	HGNC:5261													
HSPG2	gene	HSPG2	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Schwartz-Jampel syndrome, type 1, 255800 (3)						False	3	0;0;0	0.109	False		ENSG00000142798	ENSG00000142798	HGNC:5273													
HTRA2	gene	HTRA2	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	3-methylglutaconic aciduria, type VIII, 617248 (3), Autosomal recessive						False	3	0;0;0	0.109	False		ENSG00000115317	ENSG00000115317	HGNC:14348													
HUWE1	gene	HUWE1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	X-LINKED: hemizygous mutation in males, biallelic mutations in females	Mental retardation, X-linked syndromic, Turner type, 300706 (3)						False	3	0;0;0	0.109	False		ENSG00000086758	ENSG00000086758	HGNC:30892													
HYDIN	gene	HYDIN	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Ciliary dyskinesia, primary, 5, 608647 (3)						False	3	0;0;0	0.109	False		ENSG00000157423	ENSG00000157423	HGNC:19368													
HYLS1	gene	HYLS1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Hydrolethalus syndrome, 236680 (3)						False	3	0;0;0	0.109	False		ENSG00000198331	ENSG00000198331	HGNC:26558													
IARS	gene	IARS	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Growth retardation, intellectual developmental disorder, hypotonia, and hepatopathy, 617093 (3), Autosomal recessive						False	3	0;0;0	0.109	False		ENSG00000196305	ENSG00000196305	HGNC:5330													
IARS2	gene	IARS2	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	?Cataracts, growth hormone deficiency, sensory neuropathy, sensorineural hearing loss, and skeletal dysplasia						False	3	0;0;0	0.109	False		ENSG00000067704	ENSG00000067704	HGNC:29685													
IBA57	gene	IBA57	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Multiple mitochondrial dysfunctions syndrome 3, 615330 (3), Autosomal recessive						False	3	0;0;0	0.109	False		ENSG00000181873	ENSG00000181873	HGNC:27302													
ICOS	gene	ICOS	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Immunodeficiency, common variable, 1, 607594 (3)						False	3	0;0;0	0.109	False		ENSG00000163600	ENSG00000163600	HGNC:5351													
IDS	gene	IDS	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	X-LINKED: hemizygous mutation in males, biallelic mutations in females	Mucopolysaccharidosis II, 309900 (3)						False	3	0;0;0	0.109	False		ENSG00000010404	ENSG00000010404	HGNC:5389													
IDUA	gene	IDUA	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Mucopolysaccharidosis Ih, 607014 (3)						False	3	0;0;0	0.109	False		ENSG00000127415	ENSG00000127415	HGNC:5391													
IER3IP1	gene	IER3IP1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Microcephaly, epilepsy, and diabetes syndrome, 614231 (3)						False	3	0;0;0	0.109	False		ENSG00000134049	ENSG00000134049	HGNC:18550													
IFNGR1	gene	IFNGR1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Immunodeficiency 27A, mycobacteriosis, AR, 209950 (3)						False	3	0;0;0	0.109	False		ENSG00000027697	ENSG00000027697	HGNC:5439													
IFNGR2	gene	IFNGR2	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Immunodeficiency 28, mycobacteriosis, 614889 (3)						False	3	0;0;0	0.109	False		ENSG00000159128	ENSG00000159128	HGNC:5440													
IFT122	gene	IFT122	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Cranioectodermal dysplasia 1, 218330 (3)						False	3	0;0;0	0.109	False		ENSG00000163913	ENSG00000163913	HGNC:13556													
IFT140	gene	IFT140	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Short-rib thoracic dysplasia 9 with or without polydactyly, 266920 (3)						False	3	0;0;0	0.109	False		ENSG00000187535	ENSG00000187535	HGNC:29077													
IFT172	gene	IFT172	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Short-rib thoracic dysplasia 10 with or without polydactyly, 615630 (3)						False	3	0;0;0	0.109	False		ENSG00000138002	ENSG00000138002	HGNC:30391													
IFT80	gene	IFT80	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Short-rib thoracic dysplasia 2 with or without polydactyly, 611263 (3)						False	3	0;0;0	0.109	False		ENSG00000068885	ENSG00000068885	HGNC:29262													
IGF1R	gene	IGF1R	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Insulin-like growth factor I, resistance to, 270450 (3)						False	3	0;0;0	0.109	False		ENSG00000140443	ENSG00000140443	HGNC:5465													
IGFBP7	gene	IGFBP7	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Retinal arterial macroaneurysm with supravalvular pulmonic stenosis, 614224 (3)						False	3	0;0;100	0.109	False		ENSG00000163453	ENSG00000163453	HGNC:5476													
IGHM	gene	IGHM	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Agammaglobulinemia 1, 601495 (3)						False	3	0;0;0	0.109	False		ENSG00000211899	ENSG00000211899	HGNC:5541													
IGHMBP2	gene	IGHMBP2	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Neuronopathy, distal hereditary motor, type VI, 604320 (3)						False	3	0;0;0	0.109	False		ENSG00000132740	ENSG00000132740	HGNC:5542													
IKBKB	gene	IKBKB	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Immunodeficiency 15, 615592 (3)						False	3	0;0;0	0.109	False		ENSG00000104365	ENSG00000104365	HGNC:5960													
IKBKG	gene	IKBKG	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	X-LINKED: hemizygous mutation in males, biallelic mutations in females	Ectodermal, dysplasia, anhidrotic, lymphedema and immunodeficiency, 300301 (3)						False	3	0;0;0	0.109	False		ENSG00000073009	ENSG00000269335	HGNC:5961													
IL10RA	gene	IL10RA	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Inflammatory bowel disease 28, early onset, autosomal recessive, 613148 (3)						False	3	0;0;0	0.109	False		ENSG00000110324	ENSG00000110324	HGNC:5964													
IL10RB	gene	IL10RB	Expert Review;Expert Review Green	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Inflammatory bowel disease 25, early onset, #MIM612657				22549091		False	3	100;0;0	0.109	True		ENSG00000243646	ENSG00000243646	HGNC:5965													
IL11RA	gene	IL11RA	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Craniosynostosis and dental anomalies, 614188 (3)						False	3	0;0;0	0.109	False		ENSG00000137070	ENSG00000137070	HGNC:5967													
IL12RB1	gene	IL12RB1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Immunodeficiency 30, 614891 (3)						False	3	0;0;0	0.109	False		ENSG00000096996	ENSG00000096996	HGNC:5971													
IL17RA	gene	IL17RA	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Immunodeficiency 51, 613953 (3), Autosomal recessive						False	3	0;0;0	0.109	False		ENSG00000177663	ENSG00000177663	HGNC:5985													
IL1RAPL1	gene	IL1RAPL1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	X-LINKED: hemizygous mutation in males, biallelic mutations in females	Mental retardation, X-linked 21/34, 300143 (3)						False	3	0;0;0	0.109	False		ENSG00000169306	ENSG00000169306	HGNC:5996													
IL1RN	gene	IL1RN	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Interleukin 1 receptor antagonist deficiency, 612852 (3)						False	3	0;0;0	0.109	False		ENSG00000136689	ENSG00000136689	HGNC:6000													
IL2RG	gene	IL2RG	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	X-LINKED: hemizygous mutation in males, biallelic mutations in females	Severe combined immunodeficiency, X-linked, 300400 (3)						False	3	0;0;0	0.109	False		ENSG00000147168	ENSG00000147168	HGNC:6010													
IL7R	gene	IL7R	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Severe combined immunodeficiency, T-cell negative, B-cell/natural killer cell-positive type, 608971 (3)						False	3	0;0;0	0.109	False		ENSG00000168685	ENSG00000168685	HGNC:6024													
INPP5E	gene	INPP5E	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Joubert syndrome 1, 213300 (3)						False	3	0;0;0	0.109	False		ENSG00000148384	ENSG00000148384	HGNC:21474													
INPP5K	gene	INPP5K	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Muscular dystrophy, congenital, with cataracts and intellectual disability, 617404 (3), Autosomal recessive						False	3	0;0;0	0.109	False		ENSG00000132376	ENSG00000132376	HGNC:33882													
INPPL1	gene	INPPL1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Opsismodysplasia, 258480 (3)						False	3	0;0;0	0.109	False		ENSG00000165458	ENSG00000165458	HGNC:6080													
INSR	gene	INSR	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Leprechaunism, 246200 (3)						False	3	0;0;0	0.109	False		ENSG00000171105	ENSG00000171105	HGNC:6091													
INVS	gene	INVS	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Nephronophthisis 2, infantile, 602088 (3)						False	3	0;0;0	0.109	False		ENSG00000119509	ENSG00000119509	HGNC:17870													
IQCB1	gene	IQCB1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Senior-Loken syndrome 5, 609254 (3)						False	3	0;0;0	0.109	False		ENSG00000173226	ENSG00000173226	HGNC:28949													
IQSEC2	gene	IQSEC2	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	X-LINKED: hemizygous mutation in males, biallelic mutations in females	Mental retardation, X-linked 1, 309530 (3)						False	3	0;0;0	0.109	False		ENSG00000124313	ENSG00000124313	HGNC:29059													
ISCA2	gene	ISCA2	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Multiple mitochondrial dysfunctions syndrome 4, 616370 (3)						False	3	0;0;0	0.109	False		ENSG00000165898	ENSG00000165898	HGNC:19857													
ISPD	gene	ISPD	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 7, 614643 (3)						False	3	0;0;0	0.109	False		ENSG00000214960	ENSG00000214960	HGNC:37276													
ITCH	gene	ITCH	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Autoimmune disease, multisystem, with facial dysmorphism, 613385 (3)						False	3	0;0;0	0.109	False		ENSG00000078747	ENSG00000078747	HGNC:13890													
ITGA6	gene	ITGA6	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Epidermolysis bullosa, junctional, with pyloric stenosis, 226730 (3)						False	3	0;0;0	0.109	False		ENSG00000091409	ENSG00000091409	HGNC:6142													
ITGB2	gene	ITGB2	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Leukocyte adhesion deficiency, 116920 (3)						False	3	0;0;0	0.109	False		ENSG00000160255	ENSG00000160255	HGNC:6155													
ITGB4	gene	ITGB4	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Epidermolysis bullosa, junctional, with pyloric atresia, 226730 (3)						False	3	0;0;0	0.109	False		ENSG00000132470	ENSG00000132470	HGNC:6158													
ITK	gene	ITK	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Lymphoproliferative syndrome 1, 613011 (3)						False	3	0;0;0	0.109	False		ENSG00000113263	ENSG00000113263	HGNC:6171													
ITPR1	gene	ITPR1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Gillespie syndrome, 206700 (3), Autosomal recessive						False	3	0;0;0	0.109	False		ENSG00000150995	ENSG00000150995	HGNC:6180													
IVD	gene	IVD	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Isovaleric acidemia, 243500 (3)						False	3	0;0;0	0.109	False		ENSG00000128928	ENSG00000128928	HGNC:6186													
JAGN1	gene	JAGN1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Neutropenia, severe congenital, 6, autosomal recessive, 616022 (3)						False	3	0;0;0	0.109	False		ENSG00000171135	ENSG00000171135	HGNC:26926													
JAK3	gene	JAK3	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	SCID, autosomal recessive, T-negative/B-positive type, 600802 (3)						False	3	0;0;0	0.109	False		ENSG00000105639	ENSG00000105639	HGNC:6193													
JAM3	gene	JAM3	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Hemorrhagic destruction of the brain, subependymal calcification, and cataracts, 613730 (3)						False	3	0;0;0	0.109	False		ENSG00000166086	ENSG00000166086	HGNC:15532													
JUP	gene	JUP	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Naxos disease, 601214 (3)						False	3	0;0;0	0.109	False		ENSG00000173801	ENSG00000173801	HGNC:6207													
KATNB1	gene	KATNB1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Lissencephaly 6, with microcephaly, 616212 (3)						False	3	0;0;0	0.109	False		ENSG00000140854	ENSG00000140854	HGNC:6217													
KCNJ1	gene	KCNJ1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Bartter syndrome, type 2, 241200 (3)						False	3	0;0;0	0.109	False		ENSG00000151704	ENSG00000151704	HGNC:6255													
KCNJ10	gene	KCNJ10	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	SESAME syndrome, 612780 (3)						False	3	0;0;0	0.109	False		ENSG00000177807	ENSG00000177807	HGNC:6256													
KCNJ11	gene	KCNJ11	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Hyperinsulinemic hypoglycemia, familial, 2, 601820 (3)						False	3	0;0;0	0.109	False		ENSG00000187486	ENSG00000187486	HGNC:6257													
KCNQ1	gene	KCNQ1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Jervell and Lange-Nielsen syndrome, 220400 (3)						False	3	0;0;0	0.109	False		ENSG00000053918	ENSG00000053918	HGNC:6294													
KCNV2	gene	KCNV2	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Retinal cone dystrophy 3B, 610356 (3)						False	3	0;0;0	0.109	False		ENSG00000168263	ENSG00000168263	HGNC:19698													
KCTD7	gene	KCTD7	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Epilepsy, progressive myoclonic 3, with or without intracellular inclusions, 611726 (3)						False	3	0;0;0	0.109	False		ENSG00000243335	ENSG00000243335	HGNC:21957													
KDM5C	gene	KDM5C	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	X-LINKED: hemizygous mutation in males, biallelic mutations in females	Mental retardation, X-linked, syndromic, Claes-Jensen type, 300534 (3)						False	3	0;0;0	0.109	False		ENSG00000126012	ENSG00000126012	HGNC:11114													
KIAA0586	gene	KIAA0586	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Short-rib thoracic dysplasia 14 with polydactyly, 616546 (3), Autosomal recessive						False	3	0;0;0	0.109	False		ENSG00000100578	ENSG00000100578	HGNC:19960													
KIAA1109	gene	KIAA1109	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Alkuraya-Kucinskas syndrome, 617822 (3), Autosomal recessive						False	3	0;0;0	0.109	False		ENSG00000138688	ENSG00000138688	HGNC:26953													
KIF14	gene	KIF14	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Microcephaly 20, primary, autosomal recessive, 617914 (3)						False	3	0;0;0	0.109	False		ENSG00000118193	ENSG00000118193	HGNC:19181													
KIF1A	gene	KIF1A	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Spastic paraplegia 30, autosomal recessive, 610357 (3)						False	3	0;0;0	0.109	False		ENSG00000130294	ENSG00000130294	HGNC:888													
KIF1BP	gene	KIF1BP	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Goldberg-Shprintzen megacolon syndrome, 609460 (3)						False	3	0;0;0	0.109	False		ENSG00000198954	ENSG00000198954	HGNC:23419													
KIF1C	gene	KIF1C	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Spastic ataxia 2, autosomal recessive, 611302 (3)						False	3	0;0;0	0.109	False		ENSG00000129250	ENSG00000129250	HGNC:6317													
KIF7	gene	KIF7	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Hydrolethalus syndrome 2, 614120 (3)						False	3	0;0;0	0.109	False		ENSG00000166813	ENSG00000166813	HGNC:30497													
KLHL40	gene	KLHL40	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Nemaline myopathy 8, autosomal recessive, 615348 (3)						False	3	0;0;0	0.109	False		ENSG00000157119	ENSG00000157119	HGNC:30372													
KLHL41	gene	KLHL41	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Nemaline myopathy 9, 615731 (3)						False	3	0;0;0	0.109	False		ENSG00000239474	ENSG00000239474	HGNC:16905													
KLHL7	gene	KLHL7	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	PERCHING syndrome, 617055 (3)						False	3	0;0;0	0.109	False		ENSG00000122550	ENSG00000122550	HGNC:15646													
KNL1	gene	KNL1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Microcephaly 4, primary, autosomal recessive, 604321 (3)						False	3	0;0;0	0.109	False		ENSG00000137812	ENSG00000137812	HGNC:24054													
KPTN	gene	KPTN	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Mental retardation, autosomal recessive 41, 615637 (3)						False	3	0;0;0	0.109	False		ENSG00000118162	ENSG00000118162	HGNC:6404													
KRT10	gene	KRT10	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Epidermolytic hyperkeratosis, 113800 (3), Autosomal recessive						False	3	0;0;0	0.109	False		ENSG00000186395	ENSG00000186395	HGNC:6413													
KRT14	gene	KRT14	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Epidermolysis bullosa simplex, recessive 1, 601001 (3)						False	3	0;0;0	0.109	False		ENSG00000186847	ENSG00000186847	HGNC:6416													
KRT5	gene	KRT5	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Epidermolysis bullosa simplex, recessive 1, 601001 (3)						False	3	0;0;0	0.109	False		ENSG00000186081	ENSG00000186081	HGNC:6442													
KRT85	gene	KRT85	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Ectodermal dysplasia 4, hair/nail type, 602032 (3)						False	3	0;0;0	0.109	False		ENSG00000135443	ENSG00000135443	HGNC:6462													
KY	gene	KY	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Myopathy, myofibrillar, 7, 617114 (3), Autosomal recessive						False	3	0;0;0	0.109	False		ENSG00000174611	ENSG00000174611	HGNC:26576													
L1CAM	gene	L1CAM	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	X-LINKED: hemizygous mutation in males, biallelic mutations in females	MASA syndrome, 303350 (3)						False	3	0;0;0	0.109	False		ENSG00000198910	ENSG00000198910	HGNC:6470													
L2HGDH	gene	L2HGDH	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	L-2-hydroxyglutaric aciduria, 236792 (3)						False	3	0;0;0	0.109	False		ENSG00000087299	ENSG00000087299	HGNC:20499													
LAMA1	gene	LAMA1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Poretti-Boltshauser syndrome, 615960 (3)						False	3	0;0;0	0.109	False		ENSG00000101680	ENSG00000101680	HGNC:6481													
LAMA2	gene	LAMA2	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Muscular dystrophy, congenital merosin-deficient, 607855 (3)						False	3	0;0;0	0.109	False		ENSG00000196569	ENSG00000196569	HGNC:6482													
LAMA3	gene	LAMA3	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Epidermolysis bullosa, junctional, Herlitz type, 226700 (3)						False	3	0;0;0	0.109	False		ENSG00000053747	ENSG00000053747	HGNC:6483													
LAMB1	gene	LAMB1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Lissencephaly 5, 615191 (3)						False	3	0;0;0	0.109	False		ENSG00000091136	ENSG00000091136	HGNC:6486													
LAMB2	gene	LAMB2	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Pierson syndrome, 609049 (3)						False	3	0;0;0	0.109	False		ENSG00000172037	ENSG00000172037	HGNC:6487													
LAMB3	gene	LAMB3	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Epidermolysis bullosa, junctional, Herlitz type, 226700 (3)						False	3	0;0;0	0.109	False		ENSG00000196878	ENSG00000196878	HGNC:6490													
LAMC2	gene	LAMC2	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Epidermolysis bullosa, junctional, Herlitz type, 226700 (3)						False	3	0;0;0	0.109	False		ENSG00000058085	ENSG00000058085	HGNC:6493													
LAMC3	gene	LAMC3	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Cortical malformations, occipital, 614115 (3)						False	3	0;0;0	0.109	False		ENSG00000050555	ENSG00000050555	HGNC:6494													
LARGE1	gene	LARGE1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 6, 613154 (3)						False	3	0;0;0	0.109	False		ENSG00000133424	ENSG00000133424	HGNC:6511													
LARP7	gene	LARP7	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Alazami syndrome, 615071 (3)						False	3	0;0;0	0.109	False		ENSG00000174720	ENSG00000174720	HGNC:24912													
LARS	gene	LARS	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Infantile liver failure syndrome 1, MIM# 615438						False	3	0;0;0	0.109	True		ENSG00000133706	ENSG00000133706	HGNC:6512													
LARS2	gene	LARS2	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Perrault syndrome 4, 615300 (3)						False	3	0;0;0	0.109	False		ENSG00000011376	ENSG00000011376	HGNC:17095													
LAT	gene	LAT	Expert Review;Expert Review Green	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	"Immunodeficiency 52, MIM#	617514"				27242165;27522155		False	3	100;0;0	0.109	True		ENSG00000213658	ENSG00000213658	HGNC:18874													
LBR	gene	LBR	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Greenberg skeletal dysplasia, 215140 (3)						False	3	0;0;0	0.109	False		ENSG00000143815	ENSG00000143815	HGNC:6518													
LCA5	gene	LCA5	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Leber congenital amaurosis 5, 604537 (3)						False	3	0;0;0	0.109	False		ENSG00000135338	ENSG00000135338	HGNC:31923													
LCAT	gene	LCAT	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Norum disease, 245900 (3)						False	3	0;0;0	0.109	False		ENSG00000213398	ENSG00000213398	HGNC:6522													
LDHA	gene	LDHA	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Glycogen storage disease XI, 612933 (3)						False	3	0;0;0	0.109	False		ENSG00000134333	ENSG00000134333	HGNC:6535													
LDHB	gene	LDHB	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Lactate dehydrogenase-B deficiency, MIM# 614128				6383647		False	3	0;0;100	0.109	False		ENSG00000111716	ENSG00000111716	HGNC:6541													
LDLR	gene	LDLR	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	LDL cholesterol level QTL2/Hypercholesterolemia, familial						False	3	0;0;0	0.109	False		ENSG00000130164	ENSG00000130164	HGNC:6547													
LDLRAP1	gene	LDLRAP1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Hypercholesterolemia, familial, autosomal recessive, 603813 (3)						False	3	0;0;0	0.109	False		ENSG00000157978	ENSG00000157978	HGNC:18640													
LEP	gene	LEP	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Obesity, morbid, due to leptin deficiency, 614962 (3)						False	3	0;0;0	0.109	False		ENSG00000174697	ENSG00000174697	HGNC:6553													
LGI4	gene	LGI4	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Arthrogryposis multiplex congenita, neurogenic, with myelin defect, 617468 (3), Autosomal recessive						False	3	0;0;0	0.109	False		ENSG00000153902	ENSG00000153902	HGNC:18712													
LHX3	gene	LHX3	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Pituitary hormone deficiency, combined, 3, 221750 (3)						False	3	0;0;0	0.109	False		ENSG00000107187	ENSG00000107187	HGNC:6595													
LIAS	gene	LIAS	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Pyruvate dehydrogenase lipoic acid synthetase deficiency, 614462 (3)						False	3	0;0;0	0.109	False		ENSG00000121897	ENSG00000121897	HGNC:16429													
LIFR	gene	LIFR	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Stuve-Wiedemann syndrome/Schwartz-Jampel type 2 syndrome, 601559 (3)						False	3	0;0;0	0.109	False		ENSG00000113594	ENSG00000113594	HGNC:6597													
LIG4	gene	LIG4	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	LIG4 syndrome, 606593 (3)						False	3	100;0;0	0.109	False		ENSG00000174405	ENSG00000174405	HGNC:6601													
LINS1	gene	LINS1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Mental retardation, autosomal recessive 27, 614340 (3)						False	3	0;0;0	0.109	False		ENSG00000140471	ENSG00000140471	HGNC:30922													
LIPA	gene	LIPA	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Cholesteryl ester storage disease, 278000 (3)						False	3	0;0;0	0.109	False		ENSG00000107798	ENSG00000107798	HGNC:6617													
LIPC	gene	LIPC	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Hepatic lipase deficiency, 614025 (3)						False	3	0;0;0	0.109	False		ENSG00000166035	ENSG00000166035	HGNC:6619													
LIPT1	gene	LIPT1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Lipoyltransferase 1 deficiency, 616299 (3)						False	3	0;0;0	0.109	False		ENSG00000144182	ENSG00000144182	HGNC:29569													
LMAN1	gene	LMAN1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Combined factor V and VIII deficiency, 227300 (3)						False	3	0;0;0	0.109	False		ENSG00000074695	ENSG00000074695	HGNC:6631													
LMBR1	gene	LMBR1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Acheiropody, 200500 (3)						False	3	0;0;0	0.109	False		ENSG00000105983	ENSG00000105983	HGNC:13243													
LMBRD1	gene	LMBRD1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Methylmalonic aciduria and homocystinuria, cblF type, 277380 (3)						False	3	0;0;0	0.109	False		ENSG00000168216	ENSG00000168216	HGNC:23038													
LMNA	gene	LMNA	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Restrictive dermopathy, lethal, 275210 (3)						False	3	0;0;0	0.109	False		ENSG00000160789	ENSG00000160789	HGNC:6636													
LMOD3	gene	LMOD3	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Nemaline myopathy 10, 616165 (3)						False	3	0;0;0	0.109	False		ENSG00000163380	ENSG00000163380	HGNC:6649													
LONP1	gene	LONP1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	CODAS syndrome, 600373 (3)						False	3	0;0;0	0.109	False		ENSG00000196365	ENSG00000196365	HGNC:9479													
LPIN1	gene	LPIN1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Myoglobinuria, acute recurrent, autosomal recessive, 268200 (3)						False	3	0;0;0	0.109	False		ENSG00000134324	ENSG00000134324	HGNC:13345													
LPIN2	gene	LPIN2	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Majeed syndrome, 609628 (3)						False	3	0;0;0	0.109	False		ENSG00000101577	ENSG00000101577	HGNC:14450													
LPL	gene	LPL	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Lipoprotein lipase deficiency, 238600 (3)						False	3	0;0;0	0.109	False		ENSG00000175445	ENSG00000175445	HGNC:6677													
LRAT	gene	LRAT	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Leber congenital amaurosis 14, 613341 (3)						False	3	0;0;0	0.109	False		ENSG00000121207	ENSG00000121207	HGNC:6685													
LRBA	gene	LRBA	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Immunodeficiency, common variable, 8, with autoimmunity, 614700 (3)						False	3	0;0;0	0.109	False		ENSG00000198589	ENSG00000198589	HGNC:1742													
LRIG2	gene	LRIG2	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Urofacial syndrome 2, 615112 (3)						False	3	0;0;0	0.109	False		ENSG00000198799	ENSG00000198799	HGNC:20889													
LRMDA	gene	LRMDA	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Albinism, oculocutaneous, type VII, 615179 (3)						False	3	0;0;0	0.109	False		ENSG00000148655	ENSG00000148655	HGNC:23405													
LRP2	gene	LRP2	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Donnai-Barrow syndrome, 222448 (3)						False	3	0;0;0	0.109	False		ENSG00000081479	ENSG00000081479	HGNC:6694													
LRP4	gene	LRP4	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Cenani-Lenz syndactyly syndrome, 212780 (3)						False	3	0;0;0	0.109	False		ENSG00000134569	ENSG00000134569	HGNC:6696													
LRP5	gene	LRP5	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Osteoporosis-pseudoglioma syndrome, 259770 (3)						False	3	0;0;0	0.109	False		ENSG00000162337	ENSG00000162337	HGNC:6697													
LRPPRC	gene	LRPPRC	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Leigh syndrome, French-Canadian type, 220111 (3)						False	3	0;0;0	0.109	False		ENSG00000138095	ENSG00000138095	HGNC:15714													
LRRC6	gene	LRRC6	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Ciliary dyskinesia, primary, 19, 614935 (3)						False	3	0;0;0	0.109	False		ENSG00000129295	ENSG00000129295	HGNC:16725													
LRSAM1	gene	LRSAM1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Charcot-Marie-Toothe disease, axonal, type 2P, 614436 (3)						False	3	0;0;100	0.109	False		ENSG00000148356	ENSG00000148356	HGNC:25135													
LTBP3	gene	LTBP3	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Tooth agenesis, selective, 6, 613097 (3)						False	3	0;0;0	0.109	False		ENSG00000168056	ENSG00000168056	HGNC:6716													
LTBP4	gene	LTBP4	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Cutis laxa, autosomal recessive, type IC, 613177 (3)						False	3	0;0;0	0.109	False		ENSG00000090006	ENSG00000090006	HGNC:6717													
LYRM7	gene	LYRM7	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Mitochondrial complex III deficiency, nuclear type 8, 615838 (3), Autosomal recessive						False	3	0;0;0	0.109	False		ENSG00000186687	ENSG00000186687	HGNC:28072													
LYST	gene	LYST	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Chediak-Higashi syndrome, 214500 (3)						False	3	0;0;0	0.109	False		ENSG00000143669	ENSG00000143669	HGNC:1968													
LZTFL1	gene	LZTFL1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Bardet-Biedl syndrome 17, 615994 (3)						False	3	0;0;0	0.109	False		ENSG00000163818	ENSG00000163818	HGNC:6741													
MALT1	gene	MALT1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Immunodeficiency 12, 615468 (3)						False	3	0;0;0	0.109	False		ENSG00000172175	ENSG00000172175	HGNC:6819													
MAN1B1	gene	MAN1B1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Mental retardation, autosomal recessive 15, 614202 (3)						False	3	0;0;0	0.109	False		ENSG00000177239	ENSG00000177239	HGNC:6823													
MAN2B1	gene	MAN2B1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Mannosidosis, alpha-, types I and II, 248500 (3)						False	3	0;0;0	0.109	False		ENSG00000104774	ENSG00000104774	HGNC:6826													
MANBA	gene	MANBA	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Mannosidosis, beta, 248510 (3)						False	3	0;0;0	0.109	False		ENSG00000109323	ENSG00000109323	HGNC:6831													
MAOA	gene	MAOA	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	X-LINKED: hemizygous mutation in males, biallelic mutations in females	Brunner syndrome, 300615 (3)						False	3	0;0;0	0.109	False		ENSG00000189221	ENSG00000189221	HGNC:6833													
MAPKBP1	gene	MAPKBP1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Nephronophthisis 20, 617271 (3), Autosomal recessive						False	3	0;0;0	0.109	False		ENSG00000137802	ENSG00000137802	HGNC:29536													
MARS	gene	MARS	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Interstitial lung and liver disease, 615486 (3)						False	3	0;0;0	0.109	False		ENSG00000166986	ENSG00000166986	HGNC:6898													
MARS2	gene	MARS2	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Spastic ataxia 3, autosomal recessive, 611390 (3)						False	3	0;0;0	0.109	False		ENSG00000247626	ENSG00000247626	HGNC:25133													
MASP1	gene	MASP1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	3MC syndrome 1, 257920 (3)						False	3	0;0;0	0.109	False		ENSG00000127241	ENSG00000127241	HGNC:6901													
MBOAT7	gene	MBOAT7	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Mental retardation, autosomal recessive 57, 617188 (3)						False	3	0;0;0	0.109	False		ENSG00000125505	ENSG00000125505	HGNC:15505													
MBTPS2	gene	MBTPS2	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	X-LINKED: hemizygous mutation in males, biallelic mutations in females	IFAP syndrome with or without BRESHECK syndrome, 308205 (3)						False	3	0;0;0	0.109	False		ENSG00000012174	ENSG00000012174	HGNC:15455													
MC2R	gene	MC2R	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Glucocorticoid deficiency, due to ACTH unresponsiveness, 202200 (3)						False	3	0;0;0	0.109	False		ENSG00000185231	ENSG00000185231	HGNC:6930													
MCFD2	gene	MCFD2	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Factor V and factor VIII, combined deficiency of, 613625 (3)						False	3	0;0;0	0.109	False		ENSG00000180398	ENSG00000180398	HGNC:18451													
MCM4	gene	MCM4	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Natural killer cell and glucocorticoid deficiency with DNA repair defect, 609981 (3)						False	3	0;100;0	0.109	False		ENSG00000104738	ENSG00000104738	HGNC:6947													
MCOLN1	gene	MCOLN1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Mucolipidosis IV, 252650 (3)						False	3	0;0;0	0.109	False		ENSG00000090674	ENSG00000090674	HGNC:13356													
MCPH1	gene	MCPH1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Microcephaly 1, primary, autosomal recessive, 251200 (3)						False	3	0;0;0	0.109	False		ENSG00000147316	ENSG00000147316	HGNC:6954													
MECP2	gene	MECP2	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	X-LINKED: hemizygous mutation in males, biallelic mutations in females	Encephalopathy, neonatal severe, 300673 (3)						False	3	0;0;0	0.109	False		ENSG00000169057	ENSG00000169057	HGNC:6990													
MED12	gene	MED12	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	X-LINKED: hemizygous mutation in males, biallelic mutations in females	Lujan-Fryns syndrome, 309520 (3)						False	3	0;0;0	0.109	False		ENSG00000184634	ENSG00000184634	HGNC:11957													
MED17	gene	MED17	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Microcephaly, postnatal progressive, with seizures and brain atrophy, 613668 (3)						False	3	0;0;0	0.109	False		ENSG00000042429	ENSG00000042429	HGNC:2375													
MED23	gene	MED23	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Mental retardation, autosomal recessive 18, 614249 (3)						False	3	0;0;0	0.109	False		ENSG00000112282	ENSG00000112282	HGNC:2372													
MED25	gene	MED25	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Basel-Vanagait-Smirin-Yosef syndrome, 616449 (3)						False	3	0;0;0	0.109	False		ENSG00000104973	ENSG00000104973	HGNC:28845													
MEGF10	gene	MEGF10	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Myopathy, areflexia, respiratory distress, and dysphagia, early-onset, 614399 (3)						False	3	0;0;0	0.109	False		ENSG00000145794	ENSG00000145794	HGNC:29634													
MEGF8	gene	MEGF8	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Carpenter syndrome 2, 614976 (3)						False	3	0;0;0	0.109	False		ENSG00000105429	ENSG00000105429	HGNC:3233													
MERTK	gene	MERTK	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Retinitis pigmentosa 38, 613862 (3)						False	3	0;0;0	0.109	False		ENSG00000153208	ENSG00000153208	HGNC:7027													
MESP2	gene	MESP2	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Spondylocostal dysostosis 2, autosomal recessive, 608681 (3)						False	3	0;0;0	0.109	False		ENSG00000188095	ENSG00000188095	HGNC:29659													
METTL23	gene	METTL23	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Mental retardation, autosomal recessive 44, 615942 (3)						False	3	0;0;0	0.109	False		ENSG00000181038	ENSG00000181038	HGNC:26988													
MFN2	gene	MFN2	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Charcot-Marie-Tooth disease, axonal, type 2A2B, 617087 (3), Autosomal recessive						False	3	0;0;0	0.109	False		ENSG00000116688	ENSG00000116688	HGNC:16877													
MFSD2A	gene	MFSD2A	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Microcephaly 15, primary, autosomal recessive, 616486 (3), Autosomal recessive						False	3	0;0;0	0.109	False		ENSG00000168389	ENSG00000168389	HGNC:25897													
MFSD8	gene	MFSD8	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Ceroid lipofuscinosis, neuronal, 7, 610951 (3)						False	3	0;0;0	0.109	False		ENSG00000164073	ENSG00000164073	HGNC:28486													
MGAT2	gene	MGAT2	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Congenital disorder of glycosylation, type IIa, 212066 (3)						False	3	0;0;0	0.109	False		ENSG00000168282	ENSG00000168282	HGNC:7045													
MGME1	gene	MGME1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Mitochondrial DNA depletion syndrome 11, 615084 (3)						False	3	0;0;0	0.109	False		ENSG00000125871	ENSG00000125871	HGNC:16205													
MGP	gene	MGP	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Keutel syndrome, 245150 (3)						False	3	0;0;0	0.109	False		ENSG00000111341	ENSG00000111341	HGNC:7060													
MICU1	gene	MICU1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Myopathy with extrapyramidal signs, 615673 (3)						False	3	0;0;0	0.109	False		ENSG00000107745	ENSG00000107745	HGNC:1530													
MID1	gene	MID1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	X-LINKED: hemizygous mutation in males, biallelic mutations in females	Opitz GBBB syndrome, type I, 300000 (3)						False	3	0;0;0	0.109	False		ENSG00000101871	ENSG00000101871	HGNC:7095													
MKKS	gene	MKKS	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	McKusick-Kaufman syndrome, 236700 (3)						False	3	0;0;0	0.109	False		ENSG00000125863	ENSG00000125863	HGNC:7108													
MKS1	gene	MKS1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Meckel syndrome 1, 249000 (3)						False	3	0;0;0	0.109	False		ENSG00000011143	ENSG00000011143	HGNC:7121													
MLC1	gene	MLC1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Megalencephalic leukoencephalopathy with subcortical cysts, 604004 (3)						False	3	0;0;0	0.109	False		ENSG00000100427	ENSG00000100427	HGNC:17082													
MLYCD	gene	MLYCD	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Malonyl-CoA decarboxylase deficiency, 248360 (3)						False	3	0;0;0	0.109	False		ENSG00000103150	ENSG00000103150	HGNC:7150													
MMAA	gene	MMAA	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Methylmalonic aciduria, vitamin B12-responsive, 251100 (3)						False	3	0;0;0	0.109	False		ENSG00000151611	ENSG00000151611	HGNC:18871													
MMAB	gene	MMAB	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Methylmalonic aciduria, vitamin B12-responsive, due to defect in synthesis of adenosylcobalamin, cblB complementation type, 251110 (3)						False	3	0;0;0	0.109	False		ENSG00000139428	ENSG00000139428	HGNC:19331													
MMACHC	gene	MMACHC	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Methylmalonic aciduria and homocystinuria, cblC type, 277400 (3)						False	3	0;0;0	0.109	False		ENSG00000132763	ENSG00000132763	HGNC:24525													
MMADHC	gene	MMADHC	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Methylmalonic aciduria and homocystinuria, cblD type, 277410 (3)						False	3	0;0;0	0.109	False		ENSG00000168288	ENSG00000168288	HGNC:25221													
MMP2	gene	MMP2	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Multicentric osteolysis, nodulosis, and arthropathy, 259600 (3)						False	3	0;0;0	0.109	False		ENSG00000087245	ENSG00000087245	HGNC:7166													
MMP21	gene	MMP21	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Heterotaxy, visceral, 7, autosomal, 616749 (3), Autosomal recessive						False	3	0;0;0	0.109	False		ENSG00000154485	ENSG00000154485	HGNC:14357													
MOCS1	gene	MOCS1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Molybdenum cofactor deficiency A, 252150 (3)						False	3	0;0;0	0.109	False		ENSG00000124615	ENSG00000124615	HGNC:7190													
MOCS2	gene	MOCS2	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Molybdenum cofactor deficiency B, 252160 (3)						False	3	0;0;0	0.109	False		ENSG00000164172	ENSG00000164172	HGNC:7193													
MPDZ	gene	MPDZ	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Hydrocephalus, nonsyndromic, autosomal recessive 2, 615219 (3)						False	3	0;0;0	0.109	False		ENSG00000107186	ENSG00000107186	HGNC:7208													
MPI	gene	MPI	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Congenital disorder of glycosylation, type Ib, 602579 (3)						False	3	0;0;0	0.109	False		ENSG00000178802	ENSG00000178802	HGNC:7216													
MPL	gene	MPL	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Thrombocytopenia, congenital amegakaryocytic, 604498 (3)						False	3	0;0;0	0.109	False		ENSG00000117400	ENSG00000117400	HGNC:7217													
MPLKIP	gene	MPLKIP	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Trichothiodystrophy 4, nonphotosensitive, 234050 (3)						False	3	0;0;0	0.109	False		ENSG00000168303	ENSG00000168303	HGNC:16002													
MPV17	gene	MPV17	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Mitochondrial DNA depletion syndrome 6 (hepatocerebral type), 256810 (3)						False	3	0;0;0	0.109	False		ENSG00000115204	ENSG00000115204	HGNC:7224													
MPZ	gene	MPZ	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Dejerine-Sottas disease, 145900 (3)						False	3	0;0;0	0.109	False		ENSG00000158887	ENSG00000158887	HGNC:7225													
MRAP	gene	MRAP	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Glucocorticoid deficiency 2, 607398 (3)						False	3	0;0;0	0.109	False		ENSG00000170262	ENSG00000170262	HGNC:1304													
MRE11	gene	MRE11	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Ataxia-telangiectasia-like disorder, 604391 (3)						False	3	0;0;0	0.109	False		ENSG00000020922	ENSG00000020922	HGNC:7230													
MSTO1	gene	MSTO1	Expert Review;Expert Review Green	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Myopathy, mitochondrial, and ataxia, MIM#617675				31463572;30684668		False	3	100;0;0	0.109	True		ENSG00000125459	ENSG00000125459	HGNC:29678													
MTFMT	gene	MTFMT	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Combined oxidative phosphorylation deficiency 15, 614947 (3)						False	3	0;0;0	0.109	False		ENSG00000103707	ENSG00000103707	HGNC:29666													
MTHFD1	gene	MTHFD1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Combined immunodeficiency and megaloblastic anemia with or without hyperhomocysteinemia, 617780 (3), Autosomal recessive						False	3	0;0;0	0.109	False		ENSG00000100714	ENSG00000100714	HGNC:7432													
MTHFR	gene	MTHFR	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Homocystinuria due to MTHFR deficiency, 236250 (3)						False	3	0;0;0	0.109	False		ENSG00000177000	ENSG00000177000	HGNC:7436													
MTM1	gene	MTM1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	X-LINKED: hemizygous mutation in males, biallelic mutations in females	Myotubular myopathy, X-linked, 310400 (3)						False	3	0;0;0	0.109	False		ENSG00000171100	ENSG00000171100	HGNC:7448													
MTMR2	gene	MTMR2	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Charcot-Marie-Tooth disease, type 4B1, 601382 (3)						False	3	0;0;0	0.109	False		ENSG00000087053	ENSG00000087053	HGNC:7450													
MTO1	gene	MTO1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Combined oxidative phosphorylation deficiency 10, 614702 (3)						False	3	0;0;0	0.109	False		ENSG00000135297	ENSG00000135297	HGNC:19261													
MTR	gene	MTR	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Homocystinuria-megaloblastic anemia, cblG complementation type, 250940 (3)						False	3	0;0;0	0.109	False		ENSG00000116984	ENSG00000116984	HGNC:7468													
MTRR	gene	MTRR	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Homocystinuria-megaloblastic anemia, cbl E type, 236270 (3)						False	3	0;0;0	0.109	False		ENSG00000124275	ENSG00000124275	HGNC:7473													
MTTP	gene	MTTP	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Abetalipoproteinemia, 200100 (3)						False	3	0;0;0	0.109	False		ENSG00000138823	ENSG00000138823	HGNC:7467													
MUSK	gene	MUSK	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Myasthenic syndrome, congenital, 9, associated with acetylcholine receptor deficiency, 616325 (3)						False	3	0;0;0	0.109	False		ENSG00000030304	ENSG00000030304	HGNC:7525													
MUT	gene	MUT	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Methylmalonic aciduria, mut(0) type, 251000 (3)						False	3	0;0;0	0.109	False		ENSG00000146085	ENSG00000146085	HGNC:7526													
MVK	gene	MVK	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Mevalonic aciduria, 610377 (3)						False	3	0;0;0	0.109	False		ENSG00000110921	ENSG00000110921	HGNC:7530													
MYD88	gene	MYD88	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Pyogenic bacterial infections, recurrent, due to MYD88 deficiency, 612260 (3)						False	3	0;0;0	0.109	False		ENSG00000172936	ENSG00000172936	HGNC:7562													
MYMK	gene	MYMK	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Carey-Fineman-Ziter syndrome, 254940 (3), Autosomal recessive						False	3	0;0;0	0.109	False		ENSG00000187616	ENSG00000187616	HGNC:33778													
MYO5B	gene	MYO5B	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Microvillus inclusion disease, 251850 (3)						False	3	0;0;0	0.109	False		ENSG00000167306	ENSG00000167306	HGNC:7603													
MYO7A	gene	MYO7A	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Usher syndrome, type 1B, 276900 (3)						False	3	0;0;0	0.109	False		ENSG00000137474	ENSG00000137474	HGNC:7606													
NAA10	gene	NAA10	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	X-LINKED: hemizygous mutation in males, biallelic mutations in females	N-terminal acetyltransferase deficiency, 300855 (3)						False	3	0;0;0	0.109	False		ENSG00000102030	ENSG00000102030	HGNC:18704													
NAGA	gene	NAGA	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Schindler disease, type I, 609241 (3)						False	3	0;0;0	0.109	False		ENSG00000198951	ENSG00000198951	HGNC:7631													
NAGLU	gene	NAGLU	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Mucopolysaccharidosis type IIIB (Sanfilippo B), 252920 (3)						False	3	0;0;0	0.109	False		ENSG00000108784	ENSG00000108784	HGNC:7632													
NAGS	gene	NAGS	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	N-acetylglutamate synthase deficiency, 237310 (3)						False	3	0;0;0	0.109	False		ENSG00000161653	ENSG00000161653	HGNC:17996													
NALCN	gene	NALCN	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Hypotonia, infantile, with psychomotor retardation and characteristic facies, 615419 (3)						False	3	0;0;0	0.109	False		ENSG00000102452	ENSG00000102452	HGNC:19082													
NANS	gene	NANS	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Spondyloepimetaphyseal dysplasia, Camera-Genevieve type, 610442 (3), Autosomal recessive						False	3	0;0;0	0.109	False		ENSG00000095380	ENSG00000095380	HGNC:19237													
NARS2	gene	NARS2	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Combined oxidative phosphorylation deficiency 24, 616239 (3)						False	3	0;0;0	0.109	False		ENSG00000137513	ENSG00000137513	HGNC:26274													
NAXE	gene	NAXE	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Encephalopathy, progressive, early-onset, with brain edema and/or leukoencephalopathy, 617186 (3), Autosomal recessive						False	3	0;0;0	0.109	False		ENSG00000163382	ENSG00000163382	HGNC:18453													
NBAS	gene	NBAS	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Short stature, optic nerve atrophy, and Pelger-Huet anomaly, 614800 (3)						False	3	0;0;0	0.109	False		ENSG00000151779	ENSG00000151779	HGNC:15625													
NBN	gene	NBN	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Nijmegen breakage syndrome, 251260 (3)						False	3	0;0;0	0.109	False		ENSG00000104320	ENSG00000104320	HGNC:7652													
NCF1	gene	NCF1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Chronic granulomatous disease due to deficiency of NCF-1, 233700 (3)						False	3	0;0;0	0.109	False		ENSG00000158517	ENSG00000158517	HGNC:7660													
NCF2	gene	NCF2	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Chronic granulomatous disease due to deficiency of NCF-2, 233710 (3)						False	3	0;0;0	0.109	False		ENSG00000116701	ENSG00000116701	HGNC:7661													
NDE1	gene	NDE1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Lissencephaly 4 (with microcephaly), 614019 (3)						False	3	0;0;0	0.109	False		ENSG00000072864	ENSG00000072864	HGNC:17619													
NDP	gene	NDP	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	X-LINKED: hemizygous mutation in males, biallelic mutations in females	Norrie disease, 310600 (3)						False	3	0;0;0	0.109	False		ENSG00000124479	ENSG00000124479	HGNC:7678													
NDRG1	gene	NDRG1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Charcot-Marie-Tooth disease, type 4D, 601455 (3)						False	3	0;0;0	0.109	False		ENSG00000104419	ENSG00000104419	HGNC:7679													
NDUFA1	gene	NDUFA1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	X-LINKED: hemizygous mutation in males, biallelic mutations in females	Mitochondrial complex I deficiency, 252010 (3)						False	3	0;0;0	0.109	False		ENSG00000125356	ENSG00000125356	HGNC:7683													
NDUFA10	gene	NDUFA10	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Leigh syndrome, 256000 (3), Autosomal recessive, Mitochondrial						False	3	0;0;0	0.109	False		ENSG00000130414	ENSG00000130414	HGNC:7684													
NDUFA11	gene	NDUFA11	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Mitochondrial complex I deficiency, 252010 (3)						False	3	0;0;100	0.109	False		ENSG00000174886	ENSG00000174886	HGNC:20371													
NDUFAF2	gene	NDUFAF2	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Leigh syndrome, 256000 (3)						False	3	0;0;0	0.109	False		ENSG00000164182	ENSG00000164182	HGNC:28086													
NDUFAF5	gene	NDUFAF5	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Mitochondrial complex 1 deficiency, 252010 (3)						False	3	0;0;0	0.109	False		ENSG00000101247	ENSG00000101247	HGNC:15899													
NDUFAF6	gene	NDUFAF6	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Leigh syndrome due to mitochondrial complex I deficiency, 256000 (3)						False	3	0;0;0	0.109	False		ENSG00000156170	ENSG00000156170	HGNC:28625													
NDUFS1	gene	NDUFS1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Mitochondrial complex I deficiency, 252010 (3)						False	3	0;0;0	0.109	False		ENSG00000023228	ENSG00000023228	HGNC:7707													
NDUFS2	gene	NDUFS2	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Mitochondrial complex I deficiency, 252010 (3)						False	3	0;0;0	0.109	False		ENSG00000158864	ENSG00000158864	HGNC:7708													
NDUFS4	gene	NDUFS4	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Leigh syndrome, 256000 (3)						False	3	0;0;0	0.109	False		ENSG00000164258	ENSG00000164258	HGNC:7711													
NDUFS6	gene	NDUFS6	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Mitochondrial complex I deficiency, 252010 (3)						False	3	0;0;0	0.109	False		ENSG00000145494	ENSG00000145494	HGNC:7713													
NDUFS7	gene	NDUFS7	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Leigh syndrome, 256000 (3)						False	3	0;0;0	0.109	False		ENSG00000115286	ENSG00000115286	HGNC:7714													
NDUFS8	gene	NDUFS8	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Leigh syndrome due to mitochondrial complex I deficiency, 256000 (3)						False	3	0;0;0	0.109	False		ENSG00000110717	ENSG00000110717	HGNC:7715													
NDUFV1	gene	NDUFV1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Mitochondrial complex I deficiency, 252010 (3)						False	3	0;0;0	0.109	False		ENSG00000167792	ENSG00000167792	HGNC:7716													
NDUFV2	gene	NDUFV2	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Mitochondrial complex I deficiency, 252010 (3)						False	3	0;0;0	0.109	False		ENSG00000178127	ENSG00000178127	HGNC:7717													
NEB	gene	NEB	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Nemaline myopathy 2, autosomal recessive, 256030 (3)						False	3	0;0;0	0.109	False		ENSG00000183091	ENSG00000183091	HGNC:7720													
NECTIN1	gene	NECTIN1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Cleft lip/palate-ectodermal dysplasia syndrome, 225060 (3)						False	3	0;0;0	0.109	False		ENSG00000110400	ENSG00000110400	HGNC:9706													
NEK1	gene	NEK1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Short-rib thoracic dysplasia 6 with or without polydactyly, 263520 (3)						False	3	0;0;0	0.109	False		ENSG00000137601	ENSG00000137601	HGNC:7744													
NEK8	gene	NEK8	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Renal-hepatic-pancreatic dysplasia 2, 615415 (3), Autosomal recessive						False	3	0;0;0	0.109	False		ENSG00000160602	ENSG00000160602	HGNC:13387													
NEU1	gene	NEU1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Sialidosis, type I, 256550 (3)						False	3	0;0;0	0.109	False		ENSG00000204386	ENSG00000204386	HGNC:7758													
NEXMIF	gene	NEXMIF	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)	Mental retardation, X-linked 98, MIM #300912						False	3	100;0;0	0.109	True		ENSG00000050030	ENSG00000050030	HGNC:29433													
NFU1	gene	NFU1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Multiple mitochondrial dysfunctions syndrome 1, 605711 (3)						False	3	0;0;0	0.109	False		ENSG00000169599	ENSG00000169599	HGNC:16287													
NGF	gene	NGF	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Neuropathy, hereditary sensory and autonomic, type V, 608654 (3)						False	3	0;0;0	0.109	False		ENSG00000134259	ENSG00000134259	HGNC:7808													
NGLY1	gene	NGLY1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Congenital disorder of deglycosylation, 615273 (3)						False	3	0;0;0	0.109	False		ENSG00000151092	ENSG00000151092	HGNC:17646													
NHEJ1	gene	NHEJ1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Severe combined immunodeficiency with microcephaly, growth retardation, and sensitivity to ionizing radiation, 611291 (3)						False	3	0;0;0	0.109	False		ENSG00000187736	ENSG00000187736	HGNC:25737													
NHLRC1	gene	NHLRC1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Epilepsy, progressive myoclonic 2B (Lafora), 254780 (3)						False	3	0;0;0	0.109	False		ENSG00000187566	ENSG00000187566	HGNC:21576													
NHS	gene	NHS	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)	Cataract 40, X-linked, 302200 (3)						False	3	0;0;0	0.109	True		ENSG00000188158	ENSG00000188158	HGNC:7820													
NIPAL4	gene	NIPAL4	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Ichthyosis, congenital, autosomal recessive 6, 612281 (3)						False	3	0;0;0	0.109	False		ENSG00000172548	ENSG00000172548	HGNC:28018													
NKX3-2	gene	NKX3-2	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Spondylo-megaepiphyseal-metaphyseal dysplasia, 613330 (3), Autosomal recessive						False	3	0;0;0	0.109	False		ENSG00000109705	ENSG00000109705	HGNC:951													
NKX6-2	gene	NKX6-2	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Spastic ataxia 8, autosomal recessive, with hypomyelinating leukodystrophy, 617560 (3)						False	3	0;0;0	0.109	False		ENSG00000148826	ENSG00000148826	HGNC:19321													
NLGN4X	gene	NLGN4X	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	X-LINKED: hemizygous mutation in males, biallelic mutations in females	Mental retardation, X-linked, 300495 (3)						False	3	0;0;0	0.109	False		ENSG00000146938	ENSG00000146938	HGNC:14287													
NMNAT1	gene	NMNAT1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Leber congenital amaurosis 9, 608553 (3)						False	3	0;0;0	0.109	False		ENSG00000173614	ENSG00000173614	HGNC:17877													
NNT	gene	NNT	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Glucocorticoid deficiency 4, 614736 (3)						False	3	0;0;0	0.109	False		ENSG00000112992	ENSG00000112992	HGNC:7863													
NPC1	gene	NPC1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Niemann-Pick disease, type C1, 257220 (3)						False	3	0;0;0	0.109	False		ENSG00000141458	ENSG00000141458	HGNC:7897													
NPC2	gene	NPC2	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Niemann-pick disease, type C2, 607625 (3)						False	3	0;0;0	0.109	False		ENSG00000119655	ENSG00000119655	HGNC:14537													
NPHP1	gene	NPHP1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Joubert syndrome 4, 609583 (3)						False	3	0;0;0	0.109	False		ENSG00000144061	ENSG00000144061	HGNC:7905													
NPHP3	gene	NPHP3	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Meckel syndrome 7, 267010 (3)						False	3	0;0;0	0.109	False		ENSG00000113971	ENSG00000113971	HGNC:7907													
NPHP4	gene	NPHP4	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Senior-Loken syndrome 4, 606996 (3)						False	3	0;0;0	0.109	False		ENSG00000131697	ENSG00000131697	HGNC:19104													
NPHS1	gene	NPHS1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Nephrotic syndrome, type 1, 256300 (3)						False	3	0;0;0	0.109	False		ENSG00000161270	ENSG00000161270	HGNC:7908													
NPHS2	gene	NPHS2	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Nephrotic syndrome, type 2, 600995 (3)						False	3	0;0;0	0.109	False		ENSG00000116218	ENSG00000116218	HGNC:13394													
NPR2	gene	NPR2	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Acromesomelic dysplasia, Maroteaux type, 602875 (3)						False	3	0;0;0	0.109	False		ENSG00000159899	ENSG00000159899	HGNC:7944													
NR0B1	gene	NR0B1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	X-LINKED: hemizygous mutation in males, biallelic mutations in females	46XY sex reversal 2, dosage-sensitive, 300018 (3)						False	3	0;0;0	0.109	False		ENSG00000169297	ENSG00000169297	HGNC:7960													
NSDHL	gene	NSDHL	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	X-LINKED: hemizygous mutation in males, biallelic mutations in females	CK syndrome, 300831 (3)						False	3	0;0;0	0.109	False		ENSG00000147383	ENSG00000147383	HGNC:13398													
NSUN2	gene	NSUN2	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Mental retardation, autosomal recessive 5, 611091 (3)						False	3	0;0;0	0.109	False		ENSG00000037474	ENSG00000037474	HGNC:25994													
NT5C2	gene	NT5C2	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Spastic paraplegia 45, 613162 (3)						False	3	0;0;0	0.109	False		ENSG00000076685	ENSG00000076685	HGNC:8022													
NTRK1	gene	NTRK1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Insensitivity to pain, congenital, with anhidrosis, 256800 (3)						False	3	0;0;0	0.109	False		ENSG00000198400	ENSG00000198400	HGNC:8031													
NUBPL	gene	NUBPL	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Mitochondrial complex I deficiency, 252010 (3)						False	3	0;0;0	0.109	False		ENSG00000151413	ENSG00000151413	HGNC:20278													
NUP107	gene	NUP107	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Nephrotic syndrome, type 11, 616730 (3), Autosomal recessive						False	3	0;0;0	0.109	False		ENSG00000111581	ENSG00000111581	HGNC:29914													
NUP62	gene	NUP62	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Striatonigral degeneration, infantile, 271930 (3)						False	3	0;100;0	0.109	False		ENSG00000213024	ENSG00000213024	HGNC:8066													
NUP93	gene	NUP93	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Nephrotic syndrome, type 12, 616892 (3), Autosomal recessive						False	3	0;0;0	0.109	False		ENSG00000102900	ENSG00000102900	HGNC:28958													
NYX	gene	NYX	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	X-LINKED: hemizygous mutation in males, biallelic mutations in females	Night blindness, congenital stationary (complete), 1A, X-linked, MIM #310500						False	3	100;0;0	0.109	True		ENSG00000188937	ENSG00000188937	HGNC:8082													
OBSL1	gene	OBSL1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	3-M syndrome 2, 612921 (3)						False	3	0;0;0	0.109	False		ENSG00000124006	ENSG00000124006	HGNC:29092													
OCA2	gene	OCA2	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Albinism, brown oculocutaneous, 203200 (3)						False	3	0;0;0	0.109	False		ENSG00000104044	ENSG00000104044	HGNC:8101													
OCLN	gene	OCLN	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Band-like calcification with simplified gyration and polymicrogyria, 251290 (3)						False	3	0;0;0	0.109	False		ENSG00000197822	ENSG00000197822	HGNC:8104													
OCRL	gene	OCRL	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	X-LINKED: hemizygous mutation in males, biallelic mutations in females	Lowe syndrome, 309000 (3)						False	3	0;0;0	0.109	False		ENSG00000122126	ENSG00000122126	HGNC:8108													
OFD1	gene	OFD1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	X-LINKED: hemizygous mutation in males, biallelic mutations in females	Joubert syndrome 10, 300804 (3)						False	3	0;0;0	0.109	False		ENSG00000046651	ENSG00000046651	HGNC:2567													
OPA1	gene	OPA1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Behr syndrome, 210000 (3), Autosomal recessive						False	3	0;0;0	0.109	False		ENSG00000198836	ENSG00000198836	HGNC:8140													
OPA3	gene	OPA3	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	3-methylglutaconic aciduria, type III, 258501 (3)						False	3	0;0;0	0.109	False		ENSG00000125741	ENSG00000125741	HGNC:8142													
OPHN1	gene	OPHN1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	X-LINKED: hemizygous mutation in males, biallelic mutations in females	Mental retardation, X-linked, with cerebellar hypoplasia and distinctive facial appearance, 300486 (3)						False	3	0;0;0	0.109	False		ENSG00000079482	ENSG00000079482	HGNC:8148													
ORAI1	gene	ORAI1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Immunodeficiency 9, 612782 (3)						False	3	0;0;0	0.109	False		ENSG00000182500	ENSG00000276045	HGNC:25896													
ORC1	gene	ORC1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Meier-Gorlin syndrome 1, 224690 (3)						False	3	0;0;0	0.109	False		ENSG00000085840	ENSG00000085840	HGNC:8487													
ORC6	gene	ORC6	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Meier-Gorlin syndrome 3, 613803 (3)						False	3	0;0;0	0.109	False		ENSG00000091651	ENSG00000091651	HGNC:17151													
OSGEP	gene	OSGEP	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Galloway-Mowat syndrome 3, 617729 (3), Autosomal recessive						False	3	0;0;0	0.109	False		ENSG00000092094	ENSG00000092094	HGNC:18028													
OSTM1	gene	OSTM1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Osteopetrosis, autosomal recessive 5, 259720 (3)						False	3	0;0;0	0.109	False		ENSG00000081087	ENSG00000081087	HGNC:21652													
OTC	gene	OTC	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	X-LINKED: hemizygous mutation in males, biallelic mutations in females	Ornithine transcarbamylase deficiency, 311250 (3)						False	3	0;0;0	0.109	False		ENSG00000036473	ENSG00000036473	HGNC:8512													
OTUD6B	gene	OTUD6B	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Intellectual developmental disorder with dysmorphic facies, seizures, and distal limb anomalies, 617452 (3), Autosomal recessive						False	3	0;0;0	0.109	False		ENSG00000155100	ENSG00000155100	HGNC:24281													
P3H1	gene	P3H1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Osteogenesis imperfecta, type VIII, 610915 (3)						False	3	0;0;0	0.109	False		ENSG00000117385	ENSG00000117385	HGNC:19316													
PAH	gene	PAH	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Phenylketonuria, 261600 (3)						False	3	0;0;0	0.109	False		ENSG00000171759	ENSG00000171759	HGNC:8582													
PAK3	gene	PAK3	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	X-LINKED: hemizygous mutation in males, biallelic mutations in females	Mental retardation, X-linked 30/47, 300558 (3)						False	3	0;0;0	0.109	False		ENSG00000077264	ENSG00000077264	HGNC:8592													
PANK2	gene	PANK2	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Neurodegeneration with brain iron accumulation 1, 234200 (3)						False	3	0;0;0	0.109	False		ENSG00000125779	ENSG00000125779	HGNC:15894													
PAPSS2	gene	PAPSS2	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Brachyolmia 4 with mild epiphyseal and metaphyseal changes, 612847 (3)						False	3	0;0;0	0.109	False		ENSG00000198682	ENSG00000198682	HGNC:8604													
PC	gene	PC	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Pyruvate carboxylase deficiency, 266150 (3)						False	3	0;0;0	0.109	False		ENSG00000173599	ENSG00000173599	HGNC:8636													
PCCA	gene	PCCA	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Propionicacidemia, 606054 (3)						False	3	0;0;0	0.109	False		ENSG00000175198	ENSG00000175198	HGNC:8653													
PCCB	gene	PCCB	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Propionicacidemia, 606054 (3)						False	3	0;0;0	0.109	False		ENSG00000114054	ENSG00000114054	HGNC:8654													
PCDH12	gene	PCDH12	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Microcephaly, seizures, spasticity, and brain calcification, 251280 (3), Autosomal recessive						False	3	0;0;0	0.109	False		ENSG00000113555	ENSG00000113555	HGNC:8657													
PCDH15	gene	PCDH15	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Usher syndrome, type 1F, 602083 (3)						False	3	0;0;0	0.109	False		ENSG00000150275	ENSG00000150275	HGNC:14674													
PCNT	gene	PCNT	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Microcephalic osteodysplastic primordial dwarfism, type II, 210720 (3)						False	3	0;0;0	0.109	False		ENSG00000160299	ENSG00000160299	HGNC:16068													
PCSK1	gene	PCSK1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Obesity with impaired prohormone processing, 600955 (3)						False	3	0;0;0	0.109	False		ENSG00000175426	ENSG00000175426	HGNC:8743													
PCYT1A	gene	PCYT1A	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Spondylometaphyseal dysplasia with cone-rod dystrophy, 608940 (3)						False	3	0;0;0	0.109	False		ENSG00000161217	ENSG00000161217	HGNC:8754													
PDE6C	gene	PDE6C	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Cone dystrophy 4, 613093 (3)						False	3	0;0;0	0.109	False		ENSG00000095464	ENSG00000095464	HGNC:8787													
PDHA1	gene	PDHA1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	X-LINKED: hemizygous mutation in males, biallelic mutations in females	Pyruvate dehydrogenase E1-alpha deficiency						False	3	0;0;0	0.109	False		ENSG00000131828	ENSG00000131828	HGNC:8806													
PDHB	gene	PDHB	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Pyruvate dehydrogenase E1-beta deficiency, 614111 (3)						False	3	0;0;0	0.109	False		ENSG00000168291	ENSG00000168291	HGNC:8808													
PDP1	gene	PDP1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Pyruvate dehydrogenase phosphatase deficiency, 608782 (3)						False	3	0;0;0	0.109	False		ENSG00000164951	ENSG00000164951	HGNC:9279													
PEPD	gene	PEPD	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Prolidase deficiency, 170100 (3)						False	3	0;0;0	0.109	False		ENSG00000124299	ENSG00000124299	HGNC:8840													
PET100	gene	PET100	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Mitochondrial complex IV deficiency, 220110 (3)						False	3	0;0;0	0.109	False		ENSG00000229833	ENSG00000229833	HGNC:40038													
PEX1	gene	PEX1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Peroxisome biogenesis disorder 1A (Zellweger), 214100						False	3	0;0;0	0.109	False		ENSG00000127980	ENSG00000127980	HGNC:8850													
PEX10	gene	PEX10	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Peroxisome biogenesis disorder 6A (Zellweger), 614870						False	3	0;0;0	0.109	False		ENSG00000157911	ENSG00000157911	HGNC:8851													
PEX11B	gene	PEX11B	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Peroxisome biogenesis disorder 14B, 614920 (3)						False	3	0;0;0	0.109	False		ENSG00000131779	ENSG00000131779	HGNC:8853													
PEX12	gene	PEX12	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Peroxisome biogenesis disorder 3A (Zellweger), 614859						False	3	0;0;0	0.109	False		ENSG00000108733	ENSG00000108733	HGNC:8854													
PEX13	gene	PEX13	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Peroxisome biogenesis disorder 11A (Zellweger), 614883						False	3	0;0;0	0.109	False		ENSG00000162928	ENSG00000162928	HGNC:8855													
PEX16	gene	PEX16	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Peroxisome biogenesis disorder 8A, (Zellweger), 614876						False	3	0;0;0	0.109	False		ENSG00000121680	ENSG00000121680	HGNC:8857													
PEX2	gene	PEX2	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Peroxisome biogenesis disorder 5A (Zellweger), 614866						False	3	0;0;0	0.109	False		ENSG00000164751	ENSG00000164751	HGNC:9717													
PEX26	gene	PEX26	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Peroxisome biogenesis disorder 7A (Zellweger), 614872						False	3	0;0;0	0.109	False		ENSG00000215193	ENSG00000215193	HGNC:22965													
PEX3	gene	PEX3	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Peroxisome biogenesis disorder 10A (Zellweger), 614882						False	3	0;0;0	0.109	False		ENSG00000034693	ENSG00000034693	HGNC:8858													
PEX5	gene	PEX5	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Peroxisome biogenesis disorder 2A (Zellweger), 214110						False	3	0;0;0	0.109	False		ENSG00000139197	ENSG00000139197	HGNC:9719													
PEX6	gene	PEX6	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Peroxisome biogenesis disorder 4A (Zellweger), 614862						False	3	0;0;0	0.109	False		ENSG00000124587	ENSG00000124587	HGNC:8859													
PEX7	gene	PEX7	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Chondrodysplasia punctata, rhizomelic, type 1, 215100 (3)						False	3	0;0;0	0.109	False		ENSG00000112357	ENSG00000112357	HGNC:8860													
PFKM	gene	PFKM	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Glycogen storage disease VII, 232800 (3)						False	3	0;0;0	0.109	False		ENSG00000152556	ENSG00000152556	HGNC:8877													
PGAP1	gene	PGAP1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Mental retardation, autosomal recessive 42, 615802 (3), Autosomal recessive						False	3	0;0;0	0.109	False		ENSG00000197121	ENSG00000197121	HGNC:25712													
PGAP2	gene	PGAP2	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Hyperphosphatasia with mental retardation syndrome 3, 614207 (3)						False	3	0;0;0	0.109	False		ENSG00000148985	ENSG00000148985	HGNC:17893													
PGAP3	gene	PGAP3	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Hyperphosphatasia with mental retardation syndrome 4, 615716 (3)						False	3	0;0;0	0.109	False		ENSG00000161395	ENSG00000161395	HGNC:23719													
PGK1	gene	PGK1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	X-LINKED: hemizygous mutation in males, biallelic mutations in females	Phosphoglycerate kinase 1 deficiency, 300653 (3)						False	3	0;0;0	0.109	False		ENSG00000102144	ENSG00000102144	HGNC:8896													
PGM1	gene	PGM1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Congenital disorder of glycosylation, type It, 614921 (3)						False	3	0;0;0	0.109	False		ENSG00000079739	ENSG00000079739	HGNC:8905													
PGM3	gene	PGM3	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Immunodeficiency 23, 615816 (3)						False	3	0;0;0	0.109	False		ENSG00000013375	ENSG00000013375	HGNC:8907													
PHF6	gene	PHF6	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	X-LINKED: hemizygous mutation in males, biallelic mutations in females	Borjeson-Forssman-Lehmann syndrome, 301900 (3)						False	3	0;0;0	0.109	False		ENSG00000156531	ENSG00000156531	HGNC:18145													
PHF8	gene	PHF8	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	X-LINKED: hemizygous mutation in males, biallelic mutations in females	Mental retardation syndrome, X-linked, Siderius type, 300263 (3)						False	3	0;0;0	0.109	False		ENSG00000172943	ENSG00000172943	HGNC:20672													
PHGDH	gene	PHGDH	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Neu-Laxova syndrome1, 256520 (3)						False	3	0;0;0	0.109	False		ENSG00000092621	ENSG00000092621	HGNC:8923													
PHYH	gene	PHYH	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Refsum disease, 266500 (3)						False	3	0;0;0	0.109	False		ENSG00000107537	ENSG00000107537	HGNC:8940													
PIEZO2	gene	PIEZO2	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Arthrogryposis, distal, with impaired proprioception and touch, 617146 (3), Autosomal recessive						False	3	0;0;0	0.109	False		ENSG00000154864	ENSG00000154864	HGNC:26270													
PIGA	gene	PIGA	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	X-LINKED: hemizygous mutation in males, biallelic mutations in females	Multiple congenital anomalies-hypotonia-seizures syndrome 2, 300868 (3)						False	3	0;0;0	0.109	False		ENSG00000165195	ENSG00000165195	HGNC:8957													
PIGG	gene	PIGG	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Mental retardation, autosomal recessive 53, 616917 (3)						False	3	0;0;0	0.109	False		ENSG00000174227	ENSG00000174227	HGNC:25985													
PIGL	gene	PIGL	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	CHIME syndrome, 280000 (3)						False	3	0;0;0	0.109	False		ENSG00000108474	ENSG00000108474	HGNC:8966													
PIGN	gene	PIGN	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Multiple congenital anomalies-hypotonia-seizures syndrome 1, 614080 (3)						False	3	0;0;0	0.109	False		ENSG00000197563	ENSG00000197563	HGNC:8967													
PIGO	gene	PIGO	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Hyperphosphatasia with mental retardation syndrome 2, 614749 (3)						False	3	0;0;0	0.109	False		ENSG00000165282	ENSG00000165282	HGNC:23215													
PIGT	gene	PIGT	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Multiple congenital anomalies-hypotonia-seizures syndrome 3						False	3	0;0;0	0.109	False		ENSG00000124155	ENSG00000124155	HGNC:14938													
PIGV	gene	PIGV	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Hyperphosphatasia with mental retardation syndrome 1, 239300 (3)						False	3	0;0;0	0.109	False		ENSG00000060642	ENSG00000060642	HGNC:26031													
PIH1D3	gene	PIH1D3	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	X-LINKED: hemizygous mutation in males, biallelic mutations in females	Ciliary dyskinesia, primary, 36, X-linked, 300991 (3), X-linked recessive						False	3	0;0;0	0.109	False		ENSG00000080572	ENSG00000080572	HGNC:28570													
PKHD1	gene	PKHD1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Polycystic kidney and hepatic disease, 263200 (3)						False	3	0;0;0	0.109	False		ENSG00000170927	ENSG00000170927	HGNC:9016													
PKLR	gene	PKLR	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Pyruvate kinase deficiency, 266200 (3)						False	3	0;0;0	0.109	False		ENSG00000143627	ENSG00000143627	HGNC:9020													
PLA2G6	gene	PLA2G6	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Neurodegeneration with brain iron accumulation 2B, 610217 (3)						False	3	0;0;0	0.109	False		ENSG00000184381	ENSG00000184381	HGNC:9039													
PLAA	gene	PLAA	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Neurodevelopmental disorder with progressive microcephaly, spasticity, and brain anomalies, 617527 (3), Autosomal recessive						False	3	0;0;0	0.109	False		ENSG00000137055	ENSG00000137055	HGNC:9043													
PLCE1	gene	PLCE1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Nephrotic syndrome, type 3, 610725 (3)						False	3	0;0;0	0.109	False		ENSG00000138193	ENSG00000138193	HGNC:17175													
PLEC	gene	PLEC	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Epidermolysis bullosa simplex with pyloric atresia, 612138 (3)						False	3	0;0;0	0.109	False		ENSG00000178209	ENSG00000178209	HGNC:9069													
PLG	gene	PLG	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Plasminogen deficiency, type I, 217090 (3)						False	3	0;0;0	0.109	False		ENSG00000122194	ENSG00000122194	HGNC:9071													
PLOD1	gene	PLOD1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Ehlers-Danlos syndrome, type VI, 225400 (3)						False	3	0;0;0	0.109	False		ENSG00000083444	ENSG00000083444	HGNC:9081													
PLOD2	gene	PLOD2	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Bruck syndrome 2, 609220 (3)						False	3	0;0;0	0.109	False		ENSG00000152952	ENSG00000152952	HGNC:9082													
PLP1	gene	PLP1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	X-LINKED: hemizygous mutation in males, biallelic mutations in females	Pelizaeus-Merzbacher disease, 312080 (3)						False	3	0;0;0	0.109	False		ENSG00000123560	ENSG00000123560	HGNC:9086													
PLPBP	gene	PLPBP	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Epilepsy, early-onset, vitamin B6-dependent, 617290 (3), Autosomal recessive						False	3	0;0;0	0.109	False		ENSG00000147471	ENSG00000147471	HGNC:9457													
PMM2	gene	PMM2	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Congenital disorder of glycosylation, type Ia, 212065 (3)						False	3	0;0;0	0.109	False		ENSG00000140650	ENSG00000140650	HGNC:9115													
PMPCA	gene	PMPCA	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Spinocerebellar ataxia, autosomal recessive 2, 213200 (3)						False	3	0;0;0	0.109	False		ENSG00000165688	ENSG00000165688	HGNC:18667													
PNKP	gene	PNKP	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Microcephaly, seizures, and developmental delay, 613402 (3)						False	3	0;0;0	0.109	False		ENSG00000039650	ENSG00000039650	HGNC:9154													
PNP	gene	PNP	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Immunodeficiency due to purine nucleoside phosphorylase deficiency, 613179 (3)						False	3	0;0;0	0.109	False		ENSG00000198805	ENSG00000198805	HGNC:7892													
PNPLA6	gene	PNPLA6	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Boucher-Neuhauser syndrome, 215470 (3)						False	3	0;0;0	0.109	False		ENSG00000032444	ENSG00000032444	HGNC:16268													
PNPO	gene	PNPO	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Pyridoxamine 5'-phosphate oxidase deficiency, 610090 (3)						False	3	0;0;0	0.109	False		ENSG00000108439	ENSG00000108439	HGNC:30260													
POC1A	gene	POC1A	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Short stature, onychodysplasia, facial dysmorphism, and hypotrichosis, 614813 (3)						False	3	0;0;0	0.109	False		ENSG00000164087	ENSG00000164087	HGNC:24488													
POLG	gene	POLG	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Mitochondrial DNA depletion syndrome 4A (Alpers type), 203700 (3)						False	3	0;0;0	0.109	False		ENSG00000140521	ENSG00000140521	HGNC:9179													
POLR1C	gene	POLR1C	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Treacher Collins syndrome 3, 248390 (3)						False	3	0;0;0	0.109	False		ENSG00000171453	ENSG00000171453	HGNC:20194													
POLR3A	gene	POLR3A	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Leukodystrophy, hypomyelinating, 7, with or without oligodontia and/or hypogonadotropic hypogonadism, 607694 (3)						False	3	0;0;0	0.109	False		ENSG00000148606	ENSG00000148606	HGNC:30074													
POLR3B	gene	POLR3B	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Leukodystrophy, hypomyelinating, 8, with or without oligodontia and/or hypogonadotropic hypogonadism, 614381 (3)						False	3	0;0;0	0.109	False		ENSG00000013503	ENSG00000013503	HGNC:30348													
POMC	gene	POMC	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Obesity, adrenal insufficiency, and red hair due to POMC deficiency, 609734 (3)						False	3	0;0;0	0.109	False		ENSG00000115138	ENSG00000115138	HGNC:9201													
POMGNT1	gene	POMGNT1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 3, 253280 (3)						False	3	0;0;0	0.109	False		ENSG00000085998	ENSG00000085998	HGNC:19139													
POMGNT2	gene	POMGNT2	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies, type A, 8, 614830 (3)						False	3	0;0;0	0.109	False		ENSG00000144647	ENSG00000144647	HGNC:25902													
POMK	gene	POMK	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 12, 615249 (3)						False	3	0;0;0	0.109	False		ENSG00000185900	ENSG00000185900	HGNC:26267													
POMP	gene	POMP	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Keratosis linearis with ichthyosis congenita and sclerosing keratoderma, 601952 (3)						False	3	0;0;0	0.109	False		ENSG00000132963	ENSG00000132963	HGNC:20330													
POMT1	gene	POMT1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 1, 236670 (3)						False	3	0;0;0	0.109	False		ENSG00000130714	ENSG00000130714	HGNC:9202													
POMT2	gene	POMT2	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 2, 613150 (3)						False	3	0;0;0	0.109	False		ENSG00000009830	ENSG00000009830	HGNC:19743													
POP1	gene	POP1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Anauxetic dysplasia 2, 617396 (3), Autosomal recessive						False	3	0;0;0	0.109	False		ENSG00000104356	ENSG00000104356	HGNC:30129													
POR	gene	POR	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Antley-Bixler syndrome with genital anomalies and disordered steroidogenesis, 201750 (3)						False	3	0;0;0	0.109	False		ENSG00000127948	ENSG00000127948	HGNC:9208													
POU1F1	gene	POU1F1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Pituitary hormone deficiency, combined, 1, 613038 (3)						False	3	0;0;0	0.109	False		ENSG00000064835	ENSG00000064835	HGNC:9210													
PPA2	gene	PPA2	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Sudden cardiac failure, infantile, 617222 (3), Autosomal recessive						False	3	0;0;0	0.109	False		ENSG00000138777	ENSG00000138777	HGNC:28883													
PPIB	gene	PPIB	Expert Review;Expert Review Green	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Osteogenesis imperfecta, type IX, #259440						False	3	100;0;0	0.109	True		ENSG00000166794	ENSG00000166794	HGNC:9255													
PPT1	gene	PPT1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Ceroid lipofuscinosis, neuronal, 1, 256730 (3)						False	3	0;0;0	0.109	False		ENSG00000131238	ENSG00000131238	HGNC:9325													
PQBP1	gene	PQBP1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	X-LINKED: hemizygous mutation in males, biallelic mutations in females	Renpenning syndrome, 309500 (3)						False	3	0;0;0	0.109	False		ENSG00000102103	ENSG00000102103	HGNC:9330													
PRDM12	gene	PRDM12	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Neuropathy, hereditary sensory and autonomic, type VIII, 616488 (3), Autosomal recessive						False	3	0;0;0	0.109	False		ENSG00000130711	ENSG00000130711	HGNC:13997													
PRDM5	gene	PRDM5	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Brittle cornea syndrome 2, 614170 (3)						False	3	0;0;0	0.109	False		ENSG00000138738	ENSG00000138738	HGNC:9349													
PRF1	gene	PRF1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Hemophagocytic lymphohistiocytosis, familial, 2, 603553 (3)						False	3	0;0;0	0.109	False		ENSG00000180644	ENSG00000180644	HGNC:9360													
PRG4	gene	PRG4	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Camptodactyly-arthropathy-coxa vara-pericarditis syndrome, 208250 (3)						False	3	0;0;0	0.109	False		ENSG00000116690	ENSG00000116690	HGNC:9364													
PRICKLE1	gene	PRICKLE1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Epilepsy, progressive myoclonic 1B, 612437 (3)						False	3	0;0;0	0.109	False		ENSG00000139174	ENSG00000139174	HGNC:17019													
PRKRA	gene	PRKRA	Expert Review;Expert Review Green	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Dystonia 16, MIM#612067				29279192;25142429		False	3	100;0;0	0.109	True		ENSG00000180228	ENSG00000180228	HGNC:9438													
PROC	gene	PROC	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Thrombophilia due to protein C deficiency, autosomal recessive, 612304 (3)						False	3	0;0;0	0.109	False		ENSG00000115718	ENSG00000115718	HGNC:9451													
PROP1	gene	PROP1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Pituitary hormone deficiency, combined, 2, 262600 (3)						False	3	0;0;0	0.109	False		ENSG00000175325	ENSG00000175325	HGNC:9455													
PROS1	gene	PROS1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Thrombophilia due to protein S deficiency, autosomal recessive, 614514 (3)						False	3	0;0;0	0.109	False		ENSG00000184500	ENSG00000184500	HGNC:9456													
PRPS1	gene	PRPS1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	X-LINKED: hemizygous mutation in males, biallelic mutations in females	Arts syndrome, 301835 (3)						False	3	0;0;0	0.109	False		ENSG00000147224	ENSG00000147224	HGNC:9462													
PRUNE1	gene	PRUNE1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Neurodevelopmental disorder with microcephaly, hypotonia, and variable brain anomalies, 617481 (3), Autosomal recessive						False	3	0;0;0	0.109	False		ENSG00000143363	ENSG00000143363	HGNC:13420													
PRX	gene	PRX	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Dejerine-Sottas disease, 145900 (3)						False	3	0;0;0	0.109	False		ENSG00000105227	ENSG00000105227	HGNC:13797													
PSAP	gene	PSAP	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Metachromatic leukodystrophy due to SAP-b deficiency, 249900 (3)						False	3	0;0;0	0.109	False		ENSG00000197746	ENSG00000197746	HGNC:9498													
PSAT1	gene	PSAT1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Neu-Laxova syndrome 2, 616038 (3)						False	3	0;0;0	0.109	False		ENSG00000135069	ENSG00000135069	HGNC:19129													
PSMB8	gene	PSMB8	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Autoinflammation, lipodystrophy, and dermatosis syndrome, 256040 (3)						False	3	0;0;0	0.109	False		ENSG00000204264	ENSG00000204264	HGNC:9545													
PSPH	gene	PSPH	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Phosphoserine phosphatase deficiency, 614023 (3)						False	3	0;0;0	0.109	False		ENSG00000146733	ENSG00000146733	HGNC:9577													
PTH1R	gene	PTH1R	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Chondrodysplasia, Blomstrand type, 215045 (3)						False	3	0;0;0	0.109	False		ENSG00000160801	ENSG00000160801	HGNC:9608													
PTS	gene	PTS	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Hyperphenylalaninemia, BH4-deficient, A, 261640 (3)						False	3	0;0;0	0.109	False		ENSG00000150787	ENSG00000150787	HGNC:9689													
PUS1	gene	PUS1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Mitochondrial myopathy and sideroblastic anemia 1, 600462 (3)						False	3	0;0;0	0.109	False		ENSG00000177192	ENSG00000177192	HGNC:15508													
PXDN	gene	PXDN	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Corneal opacification and other ocular anomalies, 269400 (3)						False	3	0;0;0	0.109	False		ENSG00000130508	ENSG00000130508	HGNC:14966													
PYCR1	gene	PYCR1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Cutis laxa, autosomal recessive, type IIB, 612940 (3)						False	3	0;0;0	0.109	False		ENSG00000183010	ENSG00000183010	HGNC:9721													
PYCR2	gene	PYCR2	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Leukodystrophy, hypomyelinating, 10, 616420 (3)						False	3	0;0;0	0.109	False		ENSG00000143811	ENSG00000143811	HGNC:30262													
PYROXD1	gene	PYROXD1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Myopathy, myofibrillar, 8, 617258 (3), Autosomal recessive						False	3	0;0;0	0.109	False		ENSG00000121350	ENSG00000121350	HGNC:26162													
QARS	gene	QARS	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Microcephaly, progressive, seizures, and cerebral and cerebellar atrophy, 615760 (3)						False	3	0;0;0	0.109	False		ENSG00000172053	ENSG00000172053	HGNC:9751													
QDPR	gene	QDPR	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Hyperphenylalaninemia, BH4-deficient, C, 261630 (3)						False	3	0;0;0	0.109	False		ENSG00000151552	ENSG00000151552	HGNC:9752													
RAB18	gene	RAB18	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Warburg micro syndrome 3, 614222 (3)						False	3	0;0;0	0.109	False		ENSG00000099246	ENSG00000099246	HGNC:14244													
RAB23	gene	RAB23	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Carpenter syndrome, 201000 (3)						False	3	0;0;0	0.109	False		ENSG00000112210	ENSG00000112210	HGNC:14263													
RAB27A	gene	RAB27A	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Griscelli syndrome, type 2, 607624 (3)						False	3	0;0;0	0.109	False		ENSG00000069974	ENSG00000069974	HGNC:9766													
RAB33B	gene	RAB33B	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Smith-McCort dysplasia 2, 615222 (3)						False	3	0;0;0	0.109	False		ENSG00000172007	ENSG00000172007	HGNC:16075													
RAB39B	gene	RAB39B	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	X-LINKED: hemizygous mutation in males, biallelic mutations in females	Mental retardation, X-linked 72, 300271 (3)						False	3	0;0;0	0.109	False		ENSG00000155961	ENSG00000155961	HGNC:16499													
RAB3GAP1	gene	RAB3GAP1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Warburg micro syndrome 1, 600118 (3)						False	3	0;0;0	0.109	False		ENSG00000115839	ENSG00000115839	HGNC:17063													
RAB3GAP2	gene	RAB3GAP2	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Warburg micro syndrome 2, 614225 (3)						False	3	0;0;0	0.109	False		ENSG00000118873	ENSG00000118873	HGNC:17168													
RAD50	gene	RAD50	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Nijmegen breakage syndrome-like disorder, 613078 (3)						False	3	0;0;0	0.109	False		ENSG00000113522	ENSG00000113522	HGNC:9816													
RAG1	gene	RAG1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Severe combined immunodeficiency, B cell-negative, 601457 (3)						False	3	0;0;0	0.109	False		ENSG00000166349	ENSG00000166349	HGNC:9831													
RAG2	gene	RAG2	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Severe combined immunodeficiency, B cell-negative, 601457 (3)						False	3	0;0;0	0.109	False		ENSG00000175097	ENSG00000175097	HGNC:9832													
RAPSN	gene	RAPSN	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Fetal akinesia deformation sequence, 208150 (3)						False	3	0;0;0	0.109	False		ENSG00000165917	ENSG00000165917	HGNC:9863													
RARB	gene	RARB	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Microphthalmia, syndromic 12, 615524 (3), Autosomal recessive						False	3	0;0;0	0.109	False		ENSG00000077092	ENSG00000077092	HGNC:9865													
RARS	gene	RARS	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Leukodystrophy, hypomyelinating, 9, 616140 (3)						False	3	0;0;0	0.109	False		ENSG00000113643	ENSG00000113643	HGNC:9870													
RARS2	gene	RARS2	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Pontocerebellar hypoplasia, type 6, 611523 (3)						False	3	0;0;0	0.109	False		ENSG00000146282	ENSG00000146282	HGNC:21406													
RAX	gene	RAX	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Microphthalmia, isolated 3, 611038 (3)						False	3	0;0;0	0.109	False		ENSG00000134438	ENSG00000134438	HGNC:18662													
RBBP8	gene	RBBP8	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Seckel syndrome 2, 606744 (3)						False	3	0;0;0	0.109	False		ENSG00000101773	ENSG00000101773	HGNC:9891													
RBCK1	gene	RBCK1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Polyglucosan body myopathy 1 with or without immunodeficiency, 615895 (3)						False	3	0;0;0	0.109	False		ENSG00000125826	ENSG00000125826	HGNC:15864													
RBM10	gene	RBM10	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	X-LINKED: hemizygous mutation in males, biallelic mutations in females	TARP syndrome, 311900 (3)						False	3	0;0;0	0.109	False		ENSG00000182872	ENSG00000182872	HGNC:9896													
RCBTB1	gene	RCBTB1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Retinal dystrophy with or without extraocular anomalies, 617175 (3), Autosomal recessive						False	3	0;0;0	0.109	False		ENSG00000136144	ENSG00000136144	HGNC:18243													
RD3	gene	RD3	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Leber congenital amaurosis 12, 610612 (3)						False	3	0;0;0	0.109	False		ENSG00000198570	ENSG00000198570	HGNC:19689													
RDH12	gene	RDH12	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Leber congenital amaurosis 13, 612712 (3)						False	3	0;0;0	0.109	False		ENSG00000139988	ENSG00000139988	HGNC:19977													
RECQL4	gene	RECQL4	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Baller-Gerold syndrome, 218600 (3)						False	3	0;0;0	0.109	False		ENSG00000160957	ENSG00000160957	HGNC:9949													
REEP6	gene	REEP6	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Retinitis pigmentosa 77, 617304 (3), Autosomal recessive						False	3	0;0;0	0.109	False		ENSG00000115255	ENSG00000115255	HGNC:30078													
REN	gene	REN	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Renal tubular dysgenesis, 267430 (3)						False	3	0;0;0	0.109	False		ENSG00000143839	ENSG00000143839	HGNC:9958													
RETREG1	gene	RETREG1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Neuropathy, hereditary sensory and autonomic, type IIB, 613115 (3)						False	3	0;0;0	0.109	False		ENSG00000154153	ENSG00000154153	HGNC:25964													
RFT1	gene	RFT1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Congenital disorder of glycosylation, type In, 612015 (3)						False	3	0;0;0	0.109	False		ENSG00000163933	ENSG00000163933	HGNC:30220													
RFX6	gene	RFX6	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Mitchell-Riley syndrome, 615710 (3)						False	3	0;0;0	0.109	False		ENSG00000185002	ENSG00000185002	HGNC:21478													
RFXANK	gene	RFXANK	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	MHC class II deficiency, complementation group B, 209920 (3)						False	3	0;0;0	0.109	False		ENSG00000064490	ENSG00000064490	HGNC:9987													
RFXAP	gene	RFXAP	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Bare lymphocyte syndrome, type II, complementation group D, 209920 (3)						False	3	0;0;0	0.109	False		ENSG00000133111	ENSG00000133111	HGNC:9988													
RIN2	gene	RIN2	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Macrocephaly, alopecia, cutis laxa, and scoliosis, 613075 (3)						False	3	0;0;0	0.109	False		ENSG00000132669	ENSG00000132669	HGNC:18750													
RIPK4	gene	RIPK4	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Popliteal pterygium syndrome 2, lethal type, 263650 (3)						False	3	0;0;0	0.109	False		ENSG00000183421	ENSG00000183421	HGNC:496													
RLIM	gene	RLIM	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	X-LINKED: hemizygous mutation in males, biallelic mutations in females	Mental retardation, X-linked 61, 300978 (3), X-linked recessive						False	3	0;0;0	0.109	False		ENSG00000131263	ENSG00000131263	HGNC:13429													
RMND1	gene	RMND1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Combined oxidative phosphorylation deficiency 11, 614922 (3)						False	3	0;0;0	0.109	False		ENSG00000155906	ENSG00000155906	HGNC:21176													
RMRP	gene	RMRP	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Cartilage-hair hypoplasia, 250250 (3)						False	3	0;0;0	0.109	False		ENSG00000269900	ENSG00000269900	HGNC:10031													
RNASEH2A	gene	RNASEH2A	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Aicardi-Goutieres syndrome 4, 610333 (3)						False	3	0;0;0	0.109	False		ENSG00000104889	ENSG00000104889	HGNC:18518													
RNASEH2B	gene	RNASEH2B	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Aicardi-Goutieres syndrome 2, 610181 (3)						False	3	0;0;0	0.109	False		ENSG00000136104	ENSG00000136104	HGNC:25671													
RNASEH2C	gene	RNASEH2C	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Aicardi-Goutieres syndrome 3, 610329 (3)						False	3	0;0;0	0.109	False		ENSG00000172922	ENSG00000172922	HGNC:24116													
RNASET2	gene	RNASET2	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Leukoencephalopathy, cystic, without megalencephaly, 612951 (3)						False	3	0;0;0	0.109	False		ENSG00000026297	ENSG00000026297	HGNC:21686													
RNU4ATAC	gene	RNU4ATAC	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Microcephalic osteodysplastic primordial dwarfism, type I, 210710 (3)						False	3	0;0;0	0.109	False		ENSG00000264229	ENSG00000264229	HGNC:34016													
ROBO3	gene	ROBO3	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Gaze palsy, horizontal, with progressive scoliosis, 607313 (3)						False	3	0;0;0	0.109	False		ENSG00000154134	ENSG00000154134	HGNC:13433													
ROGDI	gene	ROGDI	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Kohlschutter-Tonz syndrome, 226750 (3)						False	3	0;0;0	0.109	False		ENSG00000067836	ENSG00000067836	HGNC:29478													
ROR2	gene	ROR2	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Robinow syndrome, autosomal recessive, 268310 (3)						False	3	0;0;0	0.109	False		ENSG00000169071	ENSG00000169071	HGNC:10257													
RORC	gene	RORC	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Immunodeficiency 42, 616622 (3), Autosomal recessive						False	3	0;0;0	0.109	False		ENSG00000143365	ENSG00000143365	HGNC:10260													
RP2	gene	RP2	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	X-LINKED: hemizygous mutation in males, biallelic mutations in females	Retinitis pigmentosa 2, 312600 (3)						False	3	0;0;0	0.109	False		ENSG00000102218	ENSG00000102218	HGNC:10274													
RPE65	gene	RPE65	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Leber congenital amaurosis 2, 204100 (3)						False	3	0;0;0	0.109	False		ENSG00000116745	ENSG00000116745	HGNC:10294													
RPGR	gene	RPGR	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	X-LINKED: hemizygous mutation in males, biallelic mutations in females	Macular degeneration, X-linked atrophic, 300834 (3)						False	3	0;0;0	0.109	False		ENSG00000156313	ENSG00000156313	HGNC:10295													
RPGRIP1	gene	RPGRIP1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Cone-rod dystrophy 13, 608194 (3)						False	3	0;0;0	0.109	False		ENSG00000092200	ENSG00000092200	HGNC:13436													
RPGRIP1L	gene	RPGRIP1L	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Meckel syndrome 5, 611561 (3)						False	3	0;0;0	0.109	False		ENSG00000103494	ENSG00000103494	HGNC:29168													
RPS6KA3	gene	RPS6KA3	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	X-LINKED: hemizygous mutation in males, biallelic mutations in females	Coffin-Lowry syndrome						False	3	0;0;0	0.109	False		ENSG00000177189	ENSG00000177189	HGNC:10432													
RRM2B	gene	RRM2B	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Mitochondrial DNA depletion syndrome 8A (encephalomyopathic type with renal tubulopathy), 612075 (3)						False	3	0;0;0	0.109	False		ENSG00000048392	ENSG00000048392	HGNC:17296													
RSPH1	gene	RSPH1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Ciliary dyskinesia, primary, 24, 615481 (3)						False	3	0;0;0	0.109	False		ENSG00000160188	ENSG00000160188	HGNC:12371													
RSPH4A	gene	RSPH4A	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Ciliary dyskinesia, primary, 11, 612649 (3)						False	3	0;0;0	0.109	False		ENSG00000111834	ENSG00000111834	HGNC:21558													
RSPH9	gene	RSPH9	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Ciliary dyskinesia, primary, 12, 612650 (3)						False	3	0;0;0	0.109	False		ENSG00000172426	ENSG00000172426	HGNC:21057													
RTEL1	gene	RTEL1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Dyskeratosis congenita, autosomal recessive 5, 615190 (3)						False	3	0;0;0	0.109	False		ENSG00000258366	ENSG00000258366	HGNC:15888													
RTN4IP1	gene	RTN4IP1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Optic atrophy 10 with or without ataxia, mental retardation, and seizures, 616732 (3), Autosomal recessive						False	3	0;0;0	0.109	False		ENSG00000130347	ENSG00000130347	HGNC:18647													
RTTN	gene	RTTN	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Polymicrogyria with seizures, 614833 (3)						False	3	0;0;0	0.109	False		ENSG00000176225	ENSG00000176225	HGNC:18654													
RYR1	gene	RYR1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Minicore myopathy with external ophthalmoplegia, 255320 (3)						False	3	0;0;0	0.109	False		ENSG00000196218	ENSG00000196218	HGNC:10483													
SACS	gene	SACS	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Spastic ataxia, Charlevoix-Saguenay type, 270550 (3)						False	3	0;0;0	0.109	False		ENSG00000151835	ENSG00000151835	HGNC:10519													
SAMD9	gene	SAMD9	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Tumoral calcinosis, familial, normophosphatemic, 610455 (3)						False	3	0;100;0	0.109	False		ENSG00000205413	ENSG00000205413	HGNC:1348													
SAMHD1	gene	SAMHD1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Aicardi-Goutieres syndrome 5, 612952 (3)						False	3	0;0;0	0.109	False		ENSG00000101347	ENSG00000101347	HGNC:15925													
SAR1B	gene	SAR1B	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Chylomicron retention disease, 246700 (3)						False	3	0;0;0	0.109	False		ENSG00000152700	ENSG00000152700	HGNC:10535													
SARS2	gene	SARS2	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Hyperuricemia, pulmonary hypertension, renal failure, and alkalosis, 613845 (3)						False	3	0;0;0	0.109	False		ENSG00000104835	ENSG00000104835	HGNC:17697													
SBDS	gene	SBDS	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Shwachman-Diamond syndrome, 260400 (3)						False	3	0;0;0	0.109	False		ENSG00000126524	ENSG00000126524	HGNC:19440													
SBF2	gene	SBF2	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Charcot-Marie-Tooth disease, type 4B2, 604563 (3)						False	3	0;0;0	0.109	False		ENSG00000133812	ENSG00000133812	HGNC:2135													
SC5D	gene	SC5D	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Lathosterolosis, 607330 (3)						False	3	0;0;0	0.109	False		ENSG00000109929	ENSG00000109929	HGNC:10547													
SCARB2	gene	SCARB2	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Epilepsy, progressive myoclonic 4, with or without renal failure, 254900 (3)						False	3	0;0;0	0.109	False		ENSG00000138760	ENSG00000138760	HGNC:1665													
SCARF2	gene	SCARF2	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Van den Ende-Gupta syndrome, 600920 (3)						False	3	0;0;0	0.109	False		ENSG00000244486	ENSG00000244486	HGNC:19869													
SCN9A	gene	SCN9A	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Insensitivity to pain, congenital, 243000 (3)						False	3	0;0;0	0.109	False		ENSG00000169432	ENSG00000169432	HGNC:10597													
SCNN1A	gene	SCNN1A	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Pseudohypoaldosteronism, type I, 264350 (3)						False	3	0;0;0	0.109	False		ENSG00000111319	ENSG00000111319	HGNC:10599													
SCNN1B	gene	SCNN1B	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Pseudohypoaldosteronism, type I, 264350 (3)						False	3	0;0;0	0.109	False		ENSG00000168447	ENSG00000168447	HGNC:10600													
SCO2	gene	SCO2	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency 1, 604377 (3)						False	3	0;0;0	0.109	False		ENSG00000130489	ENSG00000130489	HGNC:10604													
SCYL1	gene	SCYL1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Spinocerebellar ataxia, autosomal recessive 21, 616719 (3)						False	3	0;0;0	0.109	False		ENSG00000142186	ENSG00000142186	HGNC:14372													
SDCCAG8	gene	SDCCAG8	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Bardet-Biedl syndrome 16, 615993 (3)						False	3	0;0;0	0.109	False		ENSG00000054282	ENSG00000054282	HGNC:10671													
SDHAF1	gene	SDHAF1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Mitochondrial complex II deficiency, 252011 (3)						False	3	0;0;0	0.109	False		ENSG00000205138	ENSG00000205138	HGNC:33867													
SEC23A	gene	SEC23A	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Craniolenticulosutural dysplasia, 607812 (3)						False	3	0;100;0	0.109	False		ENSG00000100934	ENSG00000100934	HGNC:10701													
SEC23B	gene	SEC23B	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Dyserythropoietic anemia, congenital, type II, 224100 (3)						False	3	0;0;0	0.109	False		ENSG00000101310	ENSG00000101310	HGNC:10702													
SELENON	gene	SELENON	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Muscular dystrophy, rigid spine, 1, 602771 (3)						False	3	0;0;0	0.109	False		ENSG00000162430	ENSG00000162430	HGNC:15999													
SEMA4A	gene	SEMA4A	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Cone-rod dystrophy 10, 610283 (3)						False	3	0;100;0	0.109	False		ENSG00000196189	ENSG00000196189	HGNC:10729													
SEPSECS	gene	SEPSECS	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Pontocerebellar hypoplasia type 2D, 613811 (3)						False	3	0;0;0	0.109	False		ENSG00000109618	ENSG00000109618	HGNC:30605													
SERAC1	gene	SERAC1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	3-methylglutaconic aciduria with deafness, encephalopathy, and Leigh-like syndrome, 614739 (3)						False	3	0;0;0	0.109	False		ENSG00000122335	ENSG00000122335	HGNC:21061													
SERPINA1	gene	SERPINA1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Emphysema-cirrhosis, due to AAT deficiency, 613490 (3)						False	3	100;0;0	0.109	True		ENSG00000197249	ENSG00000197249	HGNC:8941													
SERPINF1	gene	SERPINF1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Osteogenesis imperfecta, type VI, 613982 (3)						False	3	0;0;0	0.109	False		ENSG00000132386	ENSG00000132386	HGNC:8824													
SERPINH1	gene	SERPINH1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Orofaciodigital syndrome VI, 277170 (3)						False	3	0;0;0	0.109	False		ENSG00000149257	ENSG00000149257	HGNC:1546													
SETX	gene	SETX	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Spinocerebellar ataxia, autosomal recessive 1, 606002 (3)						False	3	0;0;0	0.109	False		ENSG00000107290	ENSG00000107290	HGNC:445													
SFTPB	gene	SFTPB	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Surfactant metabolism dysfunction, pulmonary, 1, 265120 (3)						False	3	0;0;0	0.109	False		ENSG00000168878	ENSG00000168878	HGNC:10801													
SGCA	gene	SGCA	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Muscular dystrophy, limb-girdle, type 2D, 608099 (3)						False	3	0;0;0	0.109	False		ENSG00000108823	ENSG00000108823	HGNC:10805													
SGCB	gene	SGCB	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Muscular dystrophy, limb-girdle, type 2E, 604286 (3)						False	3	0;0;0	0.109	False		ENSG00000163069	ENSG00000163069	HGNC:10806													
SGCD	gene	SGCD	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Muscular dystrophy, limb-girdle, type 2F, 601287 (3)						False	3	0;0;0	0.109	False		ENSG00000170624	ENSG00000170624	HGNC:10807													
SGCG	gene	SGCG	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Muscular dystrophy, limb-girdle, type 2C, 253700 (3)						False	3	0;0;0	0.109	False		ENSG00000102683	ENSG00000102683	HGNC:10809													
SGO1	gene	SGO1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Chronic atrial and intestinal dysrhythmia, 616201 (3)						False	3	0;0;100	0.109	False		ENSG00000129810	ENSG00000129810	HGNC:25088													
SGPL1	gene	SGPL1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Nephrotic syndrome 14, 617575 (3), Autosomal recessive						False	3	0;0;0	0.109	False		ENSG00000166224	ENSG00000166224	HGNC:10817													
SGSH	gene	SGSH	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Mucopolysaccharidisis type IIIA (Sanfilippo A), 252900 (3)						False	3	0;0;0	0.109	False		ENSG00000181523	ENSG00000181523	HGNC:10818													
SH2D1A	gene	SH2D1A	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	X-LINKED: hemizygous mutation in males, biallelic mutations in females	Lymphoproliferative syndrome, X-linked, 1, 308240 (3)						False	3	0;0;0	0.109	False		ENSG00000183918	ENSG00000183918	HGNC:10820													
SH3PXD2B	gene	SH3PXD2B	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Frank-ter Haar syndrome, 249420 (3)						False	3	0;0;0	0.109	False		ENSG00000174705	ENSG00000174705	HGNC:29242													
SH3TC2	gene	SH3TC2	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Charcot-Marie-Tooth disease, type 4C, 601596 (3)						False	3	0;0;0	0.109	False		ENSG00000169247	ENSG00000169247	HGNC:29427													
SHOX	gene	SHOX	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Langer mesomelic dysplasia, 249700 (3)						False	3	0;0;0	0.109	True		ENSG00000185960	ENSG00000185960	HGNC:10853													
SIL1	gene	SIL1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Marinesco-Sjogren syndrome, 248800 (3)						False	3	0;0;0	0.109	False		ENSG00000120725	ENSG00000120725	HGNC:24624													
SKIV2L	gene	SKIV2L	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Trichohepatoenteric syndrome 2, 614602 (3)						False	3	0;0;0	0.109	False		ENSG00000204351	ENSG00000204351	HGNC:10898													
SLC12A1	gene	SLC12A1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Bartter syndrome, type 1, 601678 (3)						False	3	0;0;0	0.109	False		ENSG00000074803	ENSG00000074803	HGNC:10910													
SLC12A5	gene	SLC12A5	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Epileptic encephalopathy, early infantile, 34, 616645 (3), Autosomal recessive						False	3	0;0;0	0.109	False		ENSG00000124140	ENSG00000124140	HGNC:13818													
SLC12A6	gene	SLC12A6	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Agenesis of the corpus callosum with peripheral neuropathy, 218000 (3)						False	3	0;0;0	0.109	False		ENSG00000140199	ENSG00000140199	HGNC:10914													
SLC13A5	gene	SLC13A5	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Epileptic encephalopathy, early infantile, 25, 615905 (3)						False	3	0;0;0	0.109	False		ENSG00000141485	ENSG00000141485	HGNC:23089													
SLC16A1	gene	SLC16A1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Monocarboxylate transporter 1 deficiency, 616095 (3)						False	3	0;0;0	0.109	False		ENSG00000155380	ENSG00000155380	HGNC:10922													
SLC16A2	gene	SLC16A2	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	X-LINKED: hemizygous mutation in males, biallelic mutations in females	Allan-Herndon-Dudley syndrome						False	3	0;0;0	0.109	False		ENSG00000147100	ENSG00000147100	HGNC:10923													
SLC17A5	gene	SLC17A5	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Sialic acid storage disorder, infantile, 269920 (3)						False	3	0;0;0	0.109	False		ENSG00000119899	ENSG00000119899	HGNC:10933													
SLC19A2	gene	SLC19A2	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Thiamine-responsive megaloblastic anemia syndrome, 249270 (3)						False	3	0;0;0	0.109	False		ENSG00000117479	ENSG00000117479	HGNC:10938													
SLC19A3	gene	SLC19A3	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Thiamine metabolism dysfunction syndrome 2 (biotin- or thiamine-responsive encephalopathy type 2), 607483 (3)						False	3	0;0;0	0.109	False		ENSG00000135917	ENSG00000135917	HGNC:16266													
SLC1A4	gene	SLC1A4	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Spastic tetraplegia, thin corpus callosum, and progressive microcephaly, 616657 (3)						False	3	0;0;0	0.109	False		ENSG00000115902	ENSG00000115902	HGNC:10942													
SLC22A5	gene	SLC22A5	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Carnitine deficiency, systemic primary, 212140 (3)						False	3	0;0;0	0.109	False		ENSG00000197375	ENSG00000197375	HGNC:10969													
SLC24A5	gene	SLC24A5	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Albinism, oculocutaneous, type VI, 113750 (3)						False	3	0;0;0	0.109	False		ENSG00000188467	ENSG00000188467	HGNC:20611													
SLC25A1	gene	SLC25A1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Combined D-2- and L-2-hydroxyglutaric aciduria, 615182 (3)						False	3	0;0;0	0.109	False		ENSG00000100075	ENSG00000100075	HGNC:10979													
SLC25A13	gene	SLC25A13	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Citrullinemia, type II, neonatal-onset, 605814 (3)						False	3	0;0;0	0.109	False		ENSG00000004864	ENSG00000004864	HGNC:10983													
SLC25A15	gene	SLC25A15	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Hyperornithinemia-hyperammonemia-homocitrullinemia syndrome, 238970 (3)						False	3	0;0;0	0.109	False		ENSG00000102743	ENSG00000102743	HGNC:10985													
SLC25A19	gene	SLC25A19	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Thiamine metabolism dysfunction syndrome 4 (progressive polyneuropathy type), 613710 (progressive polyneuropathy type), 613710						False	3	0;0;0	0.109	False		ENSG00000125454	ENSG00000125454	HGNC:14409													
SLC25A22	gene	SLC25A22	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Epileptic encephalopathy, early infantile, 3, 609304 (3)						False	3	0;0;0	0.109	False		ENSG00000177542	ENSG00000177542	HGNC:19954													
SLC25A38	gene	SLC25A38	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Anemia, sideroblastic, pyridoxine-refractory, autosomal recessive, 205950 (3)						False	3	0;0;0	0.109	False		ENSG00000144659	ENSG00000144659	HGNC:26054													
SLC25A46	gene	SLC25A46	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Neuropathy, hereditary motor and sensory, type VIB, 616505 (3), Autosomal recessive						False	3	0;0;0	0.109	False		ENSG00000164209	ENSG00000164209	HGNC:25198													
SLC26A2	gene	SLC26A2	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Achondrogenesis Ib, 600972 (3)						False	3	0;0;0	0.109	False		ENSG00000155850	ENSG00000155850	HGNC:10994													
SLC26A3	gene	SLC26A3	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Diarrhea 1, secretory chloride, congenital, 214700 (3)						False	3	0;0;0	0.109	False		ENSG00000091138	ENSG00000091138	HGNC:3018													
SLC29A3	gene	SLC29A3	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Histiocytosis-lymphadenopathy plus syndrome, 602782 (3)						False	3	0;0;0	0.109	False		ENSG00000198246	ENSG00000198246	HGNC:23096													
SLC2A10	gene	SLC2A10	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Arterial tortuosity syndrome, 208050 (3)						False	3	0;0;0	0.109	False		ENSG00000197496	ENSG00000197496	HGNC:13444													
SLC2A2	gene	SLC2A2	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Fanconi-Bickel syndrome, 227810 (3)						False	3	0;0;0	0.109	False		ENSG00000163581	ENSG00000163581	HGNC:11006													
SLC30A10	gene	SLC30A10	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Hypermanganesemia with dystonia, polycythemia, and cirrhosis, 613280 (3)						False	3	0;0;0	0.109	False		ENSG00000196660	ENSG00000196660	HGNC:25355													
SLC33A1	gene	SLC33A1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Congenital cataracts, hearing loss, and neurodegeneration, 614482 (3)						False	3	0;0;0	0.109	False		ENSG00000169359	ENSG00000169359	HGNC:95													
SLC35A3	gene	SLC35A3	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Arthrogryposis, mental retardation, and seizures (MIM615553)				24031089;28777481;28328131		False	3	100;0;0	0.109	True		ENSG00000117620	ENSG00000117620	HGNC:11023													
SLC35D1	gene	SLC35D1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Schneckenbecken dysplasia, 269250 (3)						False	3	0;0;0	0.109	False		ENSG00000116704	ENSG00000116704	HGNC:20800													
SLC37A4	gene	SLC37A4	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Glycogen storage disease Ib, 232220 (3)						False	3	0;0;0	0.109	False		ENSG00000137700	ENSG00000137700	HGNC:4061													
SLC38A8	gene	SLC38A8	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Foveal hypoplasia 2, with or without optic nerve misrouting and/or anterior segment dysgenesis, 609218 (3)						False	3	0;0;0	0.109	False		ENSG00000166558	ENSG00000166558	HGNC:32434													
SLC39A14	gene	SLC39A14	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Hypermanganesemia with dystonia 2, 617013 (3), Autosomal recessive						False	3	0;0;0	0.109	False		ENSG00000104635	ENSG00000104635	HGNC:20858													
SLC39A4	gene	SLC39A4	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Acrodermatitis enteropathica, 201100 (3)						False	3	0;0;0	0.109	False		ENSG00000147804	ENSG00000147804	HGNC:17129													
SLC39A8	gene	SLC39A8	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Congenital disorder of glycosylation, type IIn, 616721 (3), Autosomal recessive						False	3	0;0;0	0.109	False		ENSG00000138821	ENSG00000138821	HGNC:20862													
SLC45A2	gene	SLC45A2	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Albinism, oculocutaneous, type IV, 606574 (3)						False	3	0;0;0	0.109	False		ENSG00000164175	ENSG00000164175	HGNC:16472													
SLC46A1	gene	SLC46A1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Folate malabsorption, hereditary, 229050 (3)						False	3	0;0;0	0.109	False		ENSG00000076351	ENSG00000076351	HGNC:30521													
SLC4A1	gene	SLC4A1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Renal tubular acidosis, distal, AR, 611590 (3)						False	3	0;0;0	0.109	False		ENSG00000004939	ENSG00000004939	HGNC:11027													
SLC4A4	gene	SLC4A4	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Renal tubular acidosis, proximal, with ocular abnormalities, 604278 (3)						False	3	0;0;0	0.109	False		ENSG00000080493	ENSG00000080493	HGNC:11030													
SLC52A2	gene	SLC52A2	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Brown-Vialetto-Van Laere syndrome 2, 614707 (3)						False	3	0;0;0	0.109	False		ENSG00000185803	ENSG00000185803	HGNC:30224													
SLC52A3	gene	SLC52A3	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Brown-Vialetto-Van Laere syndrome 1, 211530 (3)						False	3	0;0;0	0.109	False		ENSG00000101276	ENSG00000101276	HGNC:16187													
SLC5A7	gene	SLC5A7	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Myasthenic syndrome, congenital, 20, presynaptic, 617143 (3), Autosomal recessive						False	3	0;0;0	0.109	False		ENSG00000115665	ENSG00000115665	HGNC:14025													
SLC6A3	gene	SLC6A3	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Parkinsonism-dystonia, infantile, 613135 (3)						False	3	0;0;0	0.109	False		ENSG00000142319	ENSG00000142319	HGNC:11049													
SLC6A5	gene	SLC6A5	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Hyperekplexia 3, 614618 (3)						False	3	0;0;0	0.109	False		ENSG00000165970	ENSG00000165970	HGNC:11051													
SLC6A8	gene	SLC6A8	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	X-LINKED: hemizygous mutation in males, biallelic mutations in females	Cerebral creatine deficiency syndrome 1, 300352 (3)						False	3	0;0;0	0.109	False		ENSG00000130821	ENSG00000130821	HGNC:11055													
SLC7A7	gene	SLC7A7	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Lysinuric protein intolerance, 222700 (3)						False	3	0;0;0	0.109	False		ENSG00000155465	ENSG00000155465	HGNC:11065													
SLC9A3	gene	SLC9A3	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Diarrhea 8, secretory sodium, congenital, 616868 (3), Autosomal recessive						False	3	0;0;0	0.109	False		ENSG00000066230	ENSG00000066230	HGNC:11073													
SLC9A6	gene	SLC9A6	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	X-LINKED: hemizygous mutation in males, biallelic mutations in females	Mental retardation, X-linked syndromic, Christianson type						False	3	0;0;0	0.109	False		ENSG00000198689	ENSG00000198689	HGNC:11079													
SMARCAL1	gene	SMARCAL1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Schimke immunoosseous dysplasia, 242900 (3)						False	3	0;0;0	0.109	False		ENSG00000138375	ENSG00000138375	HGNC:11102													
SMN1	gene	SMN1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Spinal muscular atrophy-1, 253300 (3)						False	3	0;0;0	0.109	False		ENSG00000172062	ENSG00000172062	HGNC:11117													
SMPD1	gene	SMPD1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Niemann-Pick disease, type A, 257200 (3)						False	3	0;0;0	0.109	False		ENSG00000166311	ENSG00000166311	HGNC:11120													
SMS	gene	SMS	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	X-LINKED: hemizygous mutation in males, biallelic mutations in females	Mental retardation, X-linked, Snyder-Robinson type, 309583 (3)						False	3	0;0;0	0.109	False		ENSG00000102172	ENSG00000102172	HGNC:11123													
SNAP29	gene	SNAP29	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma syndrome, 609528 (3)						False	3	0;0;0	0.109	False		ENSG00000099940	ENSG00000099940	HGNC:11133													
SNORD118	gene	SNORD118	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Leukoencephalopathy, brain calcifications, and cysts, 614561 (3), Autosomal recessive						False	3	0;0;100	0.109	False		ENSG00000200463	ENSG00000200463	HGNC:32952													
SNX14	gene	SNX14	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Spinocerebellar ataxia, autosomal recessive 20, 616354 (3)						False	3	0;0;0	0.109	False		ENSG00000135317	ENSG00000135317	HGNC:14977													
SOST	gene	SOST	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Sclerosteosis 1, 269500 (3)						False	3	0;0;0	0.109	False		ENSG00000167941	ENSG00000167941	HGNC:13771													
SP110	gene	SP110	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Hepatic venoocclusive disease with immunodeficiency, 235550 (3)						False	3	0;0;0	0.109	False		ENSG00000135899	ENSG00000135899	HGNC:5401													
SPAG1	gene	SPAG1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Ciliary dyskinesia, primary, 28, 615505 (3)						False	3	0;0;0	0.109	False		ENSG00000104450	ENSG00000104450	HGNC:11212													
SPART	gene	SPART	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Troyer syndrome, 275900 (3)						False	3	0;0;0	0.109	False		ENSG00000133104	ENSG00000133104	HGNC:18514													
SPATA5	gene	SPATA5	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Epilepsy, hearing loss, and mental retardation syndrome, 616577 (3), Autosomal recessive						False	3	0;0;0	0.109	False		ENSG00000145375	ENSG00000145375	HGNC:18119													
SPATA7	gene	SPATA7	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Leber congenital amaurosis 3, 604232 (3)						False	3	0;0;0	0.109	False		ENSG00000042317	ENSG00000042317	HGNC:20423													
SPEG	gene	SPEG	Expert Review;Expert Review Green	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Centronuclear myopathy 5, MIM# 615959				25087613;31625632;30412272;30157964;29614691;29474540;28624463;26578207;25087613		False	3	100;0;0	0.109	False		ENSG00000072195	ENSG00000072195	HGNC:16901													
SPG11	gene	SPG11	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Spastic paraplegia 11, autosomal recessive, 604360 (3)						False	3	0;0;0	0.109	False		ENSG00000104133	ENSG00000104133	HGNC:11226													
SPINK5	gene	SPINK5	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Netherton syndrome, 256500 (3)						False	3	0;0;0	0.109	False		ENSG00000133710	ENSG00000133710	HGNC:15464													
SPINT2	gene	SPINT2	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Diarrhea 3, secretory sodium, congenital, syndromic, 270420 (3)						False	3	0;0;0	0.109	False		ENSG00000167642	ENSG00000167642	HGNC:11247													
SPR	gene	SPR	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Dystonia, dopa-responsive, due to sepiapterin reductase deficiency, 612716 (3)						False	3	0;0;0	0.109	False		ENSG00000116096	ENSG00000116096	HGNC:11257													
SQSTM1	gene	SQSTM1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Neurodegeneration with ataxia, dystonia, and gaze palsy, childhood-onset, 617145 (3), Autosomal recessive						False	3	0;0;0	0.109	False		ENSG00000161011	ENSG00000161011	HGNC:11280													
SRD5A3	gene	SRD5A3	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Congenital disorder of glycosylation, type Iq, 612379 (3)						False	3	0;0;0	0.109	False		ENSG00000128039	ENSG00000128039	HGNC:25812													
SSR4	gene	SSR4	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	X-LINKED: hemizygous mutation in males, biallelic mutations in females	Congenital disorder of glycosylation, type Iy, 300934 (3), X-linked recessive						False	3	0;0;0	0.109	False		ENSG00000180879	ENSG00000180879	HGNC:11326													
ST3GAL5	gene	ST3GAL5	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Salt and pepper developmental regression syndrome, 609056 (3), Autosomal recessive						False	3	0;0;0	0.109	False		ENSG00000115525	ENSG00000115525	HGNC:10872													
STAMBP	gene	STAMBP	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Microcephaly-capillary malformation syndrome, 614261 (3)						False	3	0;0;0	0.109	False		ENSG00000124356	ENSG00000124356	HGNC:16950													
STAR	gene	STAR	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Lipoid adrenal hyperplasia, 201710 (3)						False	3	0;0;0	0.109	False		ENSG00000147465	ENSG00000147465	HGNC:11359													
STAT1	gene	STAT1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Immunodeficiency 31B, mycobacterial and viral infections, autosomal recessive, 613796 (3)						False	3	0;0;0	0.109	False		ENSG00000115415	ENSG00000115415	HGNC:11362													
STIL	gene	STIL	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Microcephaly 7, primary, autosomal recessive, 612703 (3)						False	3	0;0;0	0.109	False		ENSG00000123473	ENSG00000123473	HGNC:10879													
STIM1	gene	STIM1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Immunodeficiency 10, 612783 (3)						False	3	0;0;0	0.109	False		ENSG00000167323	ENSG00000167323	HGNC:11386													
STRA6	gene	STRA6	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Microphthalmia, isolated, with coloboma 8, 601186 (3)						False	3	0;0;0	0.109	False		ENSG00000137868	ENSG00000137868	HGNC:30650													
STRADA	gene	STRADA	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Polyhydramnios, megalencephaly, and symptomatic epilepsy, 611087 (3), Autosomal recessive						False	3	0;0;0	0.109	False		ENSG00000266173	ENSG00000266173	HGNC:30172													
STUB1	gene	STUB1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Spinocerebellar ataxia, autosomal recessive 16, 615768 (3)						False	3	0;0;0	0.109	False		ENSG00000103266	ENSG00000103266	HGNC:11427													
STX11	gene	STX11	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Hemophagocytic lymphohistiocytosis, familial, 4, 603552 (3)						False	3	0;0;0	0.109	False		ENSG00000135604	ENSG00000135604	HGNC:11429													
STXBP2	gene	STXBP2	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Hemophagocytic lymphohistiocytosis, familial, 5, 613101 (3)						False	3	0;0;0	0.109	False		ENSG00000076944	ENSG00000076944	HGNC:11445													
SUCLA2	gene	SUCLA2	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Mitochondrial DNA depletion syndrome 5 (encephalomyopathic with or without methylmalonic aciduria), 612073 (3)						False	3	0;0;0	0.109	False		ENSG00000136143	ENSG00000136143	HGNC:11448													
SUCLG1	gene	SUCLG1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Mitochondrial DNA depletion syndrome 9 (encephalomyopathic type with methylmalonic aciduria), 245400 (3)						False	3	0;0;0	0.109	False		ENSG00000163541	ENSG00000163541	HGNC:11449													
SUMF1	gene	SUMF1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Multiple sulfatase deficiency, 272200 (3)						False	3	0;0;0	0.109	False		ENSG00000144455	ENSG00000144455	HGNC:20376													
SUOX	gene	SUOX	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Sulfite oxidase deficiency, 272300 (3)						False	3	0;0;0	0.109	False		ENSG00000139531	ENSG00000139531	HGNC:11460													
SURF1	gene	SURF1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Leigh syndrome, due to COX deficiency, 256000 (3)						False	3	0;0;0	0.109	False		ENSG00000148290	ENSG00000148290	HGNC:11474													
SYN1	gene	SYN1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	X-LINKED: hemizygous mutation in males, biallelic mutations in females	Epilepsy, X-linked, with variable learning disabilities and behavior disorders, 300491 (3)						False	3	0;0;0	0.109	False		ENSG00000008056	ENSG00000008056	HGNC:11494													
SYP	gene	SYP	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	X-LINKED: hemizygous mutation in males, biallelic mutations in females	Mental retardation, X-linked 96, 300802 (3)						False	3	0;0;0	0.109	False		ENSG00000102003	ENSG00000102003	HGNC:11506													
TALDO1	gene	TALDO1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Transaldolase deficiency, 606003 (3)						False	3	0;0;0	0.109	False		ENSG00000177156	ENSG00000177156	HGNC:11559													
TANGO2	gene	TANGO2	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Metabolic encephalomyopathic crises, recurrent, with rhabdomyolysis, cardiac arrhythmias, and neurodegeneration						False	3	0;0;0	0.109	False		ENSG00000183597	ENSG00000183597	HGNC:25439													
TAP1	gene	TAP1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Bare lymphocyte syndrome, type I, 604571 (3)						False	3	0;0;0	0.109	False		ENSG00000168394	ENSG00000168394	HGNC:43													
TAZ	gene	TAZ	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	X-LINKED: hemizygous mutation in males, biallelic mutations in females	Barth syndrome, 302060 (3)						False	3	0;0;0	0.109	False		ENSG00000102125	ENSG00000102125	HGNC:11577													
TBC1D23	gene	TBC1D23	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Pontocerebellar hypoplasia, type 11, 617695 (3), Autosomal recessive						False	3	0;0;0	0.109	False		ENSG00000036054	ENSG00000036054	HGNC:25622													
TBC1D24	gene	TBC1D24	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Epileptic encephalopathy, early infantile, 16, 615338 (3)						False	3	0;0;0	0.109	False		ENSG00000162065	ENSG00000162065	HGNC:29203													
TBCD	gene	TBCD	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Encephalopathy, progressive, early-onset, with brain atrophy and thin corpus callosum, 617193 (3), Autosomal recessive						False	3	0;0;0	0.109	False		ENSG00000141556	ENSG00000141556	HGNC:11581													
TBCE	gene	TBCE	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Kenny-Caffey syndrome-1, 244460 (3)						False	3	0;0;0	0.109	False		ENSG00000116957	ENSG00000116957	HGNC:11582													
TBCK	gene	TBCK	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Hypotonia, infantile, with psychomotor retardation and characteristic facies 3, 616900 (3), Autosomal recessive						False	3	0;0;0	0.109	False		ENSG00000145348	ENSG00000145348	HGNC:28261													
TBX19	gene	TBX19	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Adrenocorticotropic hormone deficiency, 201400 (3)						False	3	0;0;0	0.109	False		ENSG00000143178	ENSG00000143178	HGNC:11596													
TCAP	gene	TCAP	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Muscular dystrophy, limb-girdle, type 2G, 601954 (3)						False	3	0;0;0	0.109	False		ENSG00000173991	ENSG00000173991	HGNC:11610													
TCIRG1	gene	TCIRG1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Osteopetrosis, autosomal recessive 1, 259700 (3)						False	3	0;0;0	0.109	False		ENSG00000110719	ENSG00000110719	HGNC:11647													
TCN2	gene	TCN2	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Transcobalamin II deficiency, 275350 (3)						False	3	0;0;0	0.109	False		ENSG00000185339	ENSG00000185339	HGNC:11653													
TCTN2	gene	TCTN2	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Joubert syndrome 24						False	3	0;0;0	0.109	False		ENSG00000168778	ENSG00000168778	HGNC:25774													
TCTN3	gene	TCTN3	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Joubert syndrome 18, 614815 (3)						False	3	0;0;0	0.109	False		ENSG00000119977	ENSG00000119977	HGNC:24519													
TDRD7	gene	TDRD7	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Cataract 36, 613887 (3)						False	3	0;0;0	0.109	False		ENSG00000196116	ENSG00000196116	HGNC:30831													
TELO2	gene	TELO2	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	You-Hoover-Fong syndrome, 616954 (3), Autosomal recessive						False	3	0;0;0	0.109	False		ENSG00000100726	ENSG00000100726	HGNC:29099													
TF	gene	TF	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Atransferrinemia, 209300 (3)						False	3	0;0;0	0.109	False		ENSG00000091513	ENSG00000091513	HGNC:11740													
TGM1	gene	TGM1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Ichthyosis, congenital, autosomal recessive 1, 242300 (3)						False	3	0;0;0	0.109	False		ENSG00000092295	ENSG00000092295	HGNC:11777													
TH	gene	TH	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Segawa syndrome, recessive, 605407 (3)						False	3	0;0;0	0.109	False		ENSG00000180176	ENSG00000180176	HGNC:11782													
THOC2	gene	THOC2	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	X-LINKED: hemizygous mutation in males, biallelic mutations in females	Mental retardation, X-linked 12/35, 300957 (3), X-linked recessive						False	3	0;0;0	0.109	False		ENSG00000125676	ENSG00000125676	HGNC:19073													
TIMM8A	gene	TIMM8A	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	X-LINKED: hemizygous mutation in males, biallelic mutations in females	Jensen syndrome, 311150 (3)						False	3	0;0;0	0.109	False		ENSG00000126953	ENSG00000126953	HGNC:11817													
TJP2	gene	TJP2	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Cholestasis, progressive familial intrahepatic 4, 615878 (3)						False	3	0;0;0	0.109	False		ENSG00000119139	ENSG00000119139	HGNC:11828													
TK2	gene	TK2	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Mitochondrial DNA depletion syndrome 2 (myopathic type), 609560 (3)						False	3	0;0;0	0.109	False		ENSG00000166548	ENSG00000166548	HGNC:11831													
TMCO1	gene	TMCO1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Craniofacial dysmorphism, skeletal anomalies, and mental retardation syndrome, 213980 (3)						False	3	0;0;0	0.109	False		ENSG00000143183	ENSG00000143183	HGNC:18188													
TMEM107	gene	TMEM107	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Orofaciodigital syndrome XVI, 617563 (3), Autosomal recessive						False	3	0;0;0	0.109	False		ENSG00000179029	ENSG00000179029	HGNC:28128													
TMEM126A	gene	TMEM126A	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Optic atrophy 7, 612989 (3)						False	3	0;0;0	0.109	False		ENSG00000171202	ENSG00000171202	HGNC:25382													
TMEM138	gene	TMEM138	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Joubert syndrome 16, 614465 (3)						False	3	0;0;0	0.109	False		ENSG00000149483	ENSG00000149483	HGNC:26944													
TMEM165	gene	TMEM165	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Congenital disorder of glycosylation, type IIk, 614727 (3)						False	3	0;0;0	0.109	False		ENSG00000134851	ENSG00000134851	HGNC:30760													
TMEM216	gene	TMEM216	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Joubert syndrome 2, 608091 (3)						False	3	0;0;0	0.109	False		ENSG00000187049	ENSG00000187049	HGNC:25018													
TMEM231	gene	TMEM231	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Joubert syndrome 20, 614970 (3)						False	3	0;0;0	0.109	False		ENSG00000205084	ENSG00000205084	HGNC:37234													
TMEM237	gene	TMEM237	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Joubert syndrome 14, 614424 (3)						False	3	0;0;0	0.109	False		ENSG00000155755	ENSG00000155755	HGNC:14432													
TMEM5	gene	TMEM5	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 10, 615041 (3)						False	3	0;0;0	0.109	False		ENSG00000118600	ENSG00000118600	HGNC:13530													
TMEM67	gene	TMEM67	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Joubert syndrome 6, 610688 (3)						False	3	0;0;0	0.109	False		ENSG00000164953	ENSG00000164953	HGNC:28396													
TMEM70	gene	TMEM70	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Mitochondrial complex V (ATP synthase) deficiency, nuclear type 2, 614052 (3)						False	3	0;0;0	0.109	False		ENSG00000175606	ENSG00000175606	HGNC:26050													
TMTC3	gene	TMTC3	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Lissencephaly 8, 617255 (3), Autosomal recessive						False	3	0;0;0	0.109	False		ENSG00000139324	ENSG00000139324	HGNC:26899													
TNFRSF11A	gene	TNFRSF11A	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Osteopetrosis, autosomal recessive 7, 612301 (3)						False	3	0;0;0	0.109	False		ENSG00000141655	ENSG00000141655	HGNC:11908													
TNFRSF11B	gene	TNFRSF11B	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Paget disease of bone 5, juvenile-onset, 239000 (3)						False	3	0;0;0	0.109	False		ENSG00000164761	ENSG00000164761	HGNC:11909													
TNFRSF13B	gene	TNFRSF13B	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Immunodeficiency, common variable, 2, 240500 (3)						False	3	0;0;100	0.109	False		ENSG00000240505	ENSG00000240505	HGNC:18153													
TNFSF11	gene	TNFSF11	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Osteopetrosis, autosomal recessive 2, 259710 (3)						False	3	0;0;0	0.109	False		ENSG00000120659	ENSG00000120659	HGNC:11926													
TNNT1	gene	TNNT1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Nemaline myopathy 5, Amish type, 605355 (3)						False	3	0;0;0	0.109	False		ENSG00000105048	ENSG00000105048	HGNC:11948													
TOE1	gene	TOE1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Pontocerebellar hypoplasia, type 7, 614969 (3), Autosomal recessive						False	3	0;0;0	0.109	False		ENSG00000132773	ENSG00000132773	HGNC:15954													
TPI1	gene	TPI1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Hemolytic anemia due to triosephosphate isomerase deficiency, 615512 (3)						False	3	0;0;0	0.109	False		ENSG00000111669	ENSG00000111669	HGNC:12009													
TPK1	gene	TPK1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Thiamine metabolism dysfunction syndrome 5 (episodic encephalopathy type), 614458 (3)						False	3	0;0;0	0.109	False		ENSG00000196511	ENSG00000196511	HGNC:17358													
TPM3	gene	TPM3	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Nemaline myopathy 1, autosomal dominant or recessive, 609284 (3)						False	3	0;0;0	0.109	False		ENSG00000143549	ENSG00000143549	HGNC:12012													
TPP1	gene	TPP1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Ceroid lipofuscinosis, neuronal, 2, 204500 (3)						False	3	0;0;0	0.109	False		ENSG00000166340	ENSG00000166340	HGNC:2073													
TRAPPC11	gene	TRAPPC11	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Muscular dystrophy, limb-girdle, type 2S, 615356 (3)						False	3	0;0;0	0.109	False		ENSG00000168538	ENSG00000168538	HGNC:25751													
TRAPPC9	gene	TRAPPC9	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Mental retardation, autosomal recessive 13, 613192 (3)						False	3	0;0;0	0.109	False		ENSG00000167632	ENSG00000167632	HGNC:30832													
TRDN	gene	TRDN	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Ventricular tachycardia, catecholaminergic polymorphic, 5, with or without muscle weakness, 615441 (3)						False	3	0;0;0	0.109	False		ENSG00000186439	ENSG00000186439	HGNC:12261													
TREX1	gene	TREX1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Aicardi-Goutieres syndrome 1, dominant and recessive, 225750 (3)						False	3	0;0;0	0.109	False		ENSG00000213689	ENSG00000213689	HGNC:12269													
TRIM32	gene	TRIM32	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Muscular dystrophy, limb-girdle, type 2H, 254110 (3)						False	3	0;0;0	0.109	False		ENSG00000119401	ENSG00000119401	HGNC:16380													
TRIM37	gene	TRIM37	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Mulibrey nanism, 253250 (3)						False	3	0;0;0	0.109	False		ENSG00000108395	ENSG00000108395	HGNC:7523													
TRIP11	gene	TRIP11	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Achondrogenesis, type IA, 200600 (3)						False	3	0;0;0	0.109	False		ENSG00000100815	ENSG00000100815	HGNC:12305													
TRIT1	gene	TRIT1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Combined oxidative phosphorylation deficiency 35, 617873 (3), Autosomal recessive						False	3	0;0;0	0.109	False		ENSG00000043514	ENSG00000043514	HGNC:20286													
TRMT10A	gene	TRMT10A	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Microcephaly, short stature, and impaired glucose metabolism, 616033 (3)						False	3	0;0;0	0.109	False		ENSG00000145331	ENSG00000145331	HGNC:28403													
TRMU	gene	TRMU	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Liver failure, transient infantile, 613070 (3)						False	3	0;0;0	0.109	False		ENSG00000100416	ENSG00000100416	HGNC:25481													
TRNT1	gene	TRNT1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Sideroblastic anemia with B-cell immunodeficiency, periodic fevers, and developmental delay, 616084 (3)						False	3	0;0;0	0.109	False		ENSG00000072756	ENSG00000072756	HGNC:17341													
TRPM6	gene	TRPM6	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Hypomagnesemia 1, intestinal, 602014 (3)						False	3	0;0;0	0.109	False		ENSG00000119121	ENSG00000119121	HGNC:17995													
TSEN2	gene	TSEN2	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Pontocerebellar hypoplasia type 2B, 612389 (3)						False	3	0;0;0	0.109	False		ENSG00000154743	ENSG00000154743	HGNC:28422													
TSEN54	gene	TSEN54	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Pontocerebellar hypoplasia type 2A, 277470 (3)						False	3	0;0;0	0.109	False		ENSG00000182173	ENSG00000182173	HGNC:27561													
TSFM	gene	TSFM	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Combined oxidative phosphorylation deficiency 3, 610505 (3)						False	3	0;0;0	0.109	False		ENSG00000123297	ENSG00000123297	HGNC:12367													
TSHB	gene	TSHB	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Hypothryoidism, congenital, nongoitrous 4, 275100 (3)						False	3	0;0;0	0.109	False		ENSG00000134200	ENSG00000134200	HGNC:12372													
TSPAN7	gene	TSPAN7	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	X-LINKED: hemizygous mutation in males, biallelic mutations in females	Mental retardation, X-linked 58, 300210 (3)						False	3	0;0;100	0.109	False		ENSG00000156298	ENSG00000156298	HGNC:11854													
TTC19	gene	TTC19	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Mitochondrial complex III deficiency, nuclear type 2, 615157 (3)						False	3	0;0;0	0.109	False		ENSG00000011295	ENSG00000011295	HGNC:26006													
TTC21B	gene	TTC21B	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Short-rib thoracic dysplasia 4 with or without polydactyly, 613819 (3)						False	3	0;0;0	0.109	False		ENSG00000123607	ENSG00000123607	HGNC:25660													
TTC37	gene	TTC37	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Trichohepatoenteric syndrome 1, 222470 (3)						False	3	0;0;0	0.109	False		ENSG00000198677	ENSG00000198677	HGNC:23639													
TTC7A	gene	TTC7A	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Gastrointestinal defects and immunodeficiency syndrome, 243150 (3)						False	3	0;0;0	0.109	False		ENSG00000068724	ENSG00000068724	HGNC:19750													
TTC8	gene	TTC8	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Bardet-Biedl syndrome 8, 615985 (3)						False	3	0;0;0	0.109	False		ENSG00000165533	ENSG00000165533	HGNC:20087													
TTI2	gene	TTI2	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Mental retardation, autosomal recessive 39, 615541 (3)						False	3	0;0;0	0.109	False		ENSG00000129696	ENSG00000129696	HGNC:26262													
TTN	gene	TTN	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Myopathy, early-onset, with fatal cardiomyopathy, 611705 (3)						False	3	0;0;0	0.109	False		ENSG00000155657	ENSG00000155657	HGNC:12403													
TTPA	gene	TTPA	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Ataxia with isolated vitamin E deficiency, 277460 (3)						False	3	0;0;0	0.109	False		ENSG00000137561	ENSG00000137561	HGNC:12404													
TUBGCP4	gene	TUBGCP4	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Microcephaly and chorioretinopathy, autosomal recessive, 3, 616335 (3)						False	3	0;0;0	0.109	False		ENSG00000137822	ENSG00000137822	HGNC:16691													
TUBGCP6	gene	TUBGCP6	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Microcephaly and chorioretinopathy, autosomal recessive, 1, 251270 (3)						False	3	0;0;0	0.109	False		ENSG00000128159	ENSG00000128159	HGNC:18127													
TUFM	gene	TUFM	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Combined oxidative phosphorylation deficiency 4, 610678 (3)						False	3	0;0;0	0.109	False		ENSG00000178952	ENSG00000178952	HGNC:12420													
TULP1	gene	TULP1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Retinitis pigmentosa 14, 600132 (3)						False	3	0;0;0	0.109	False		ENSG00000112041	ENSG00000112041	HGNC:12423													
TUSC3	gene	TUSC3	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Mental retardation, autosomal recessive 7, 611093 (3)						False	3	0;0;0	0.109	False		ENSG00000104723	ENSG00000104723	HGNC:30242													
TWNK	gene	TWNK	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Mitochondrial DNA depletion syndrome 7 (hepatocerebral type), 271245 (3)						False	3	0;0;0	0.109	False		ENSG00000107815	ENSG00000107815	HGNC:1160													
TXNL4A	gene	TXNL4A	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Burn-McKeown syndrome, 608572 (3)						False	3	0;100;0	0.109	False		ENSG00000141759	ENSG00000141759	HGNC:30551													
TYK2	gene	TYK2	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Immunodeficiency 35, 611521 (3)						False	3	0;0;0	0.109	False		ENSG00000105397	ENSG00000105397	HGNC:12440													
TYMP	gene	TYMP	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Mitochondrial DNA depletion syndrome 1 (MNGIE type), 603041 (3)						False	3	0;0;0	0.109	False		ENSG00000025708	ENSG00000025708	HGNC:3148													
TYR	gene	TYR	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Albinism, oculocutaneous, type IA, 203100 (3)						False	3	0;0;0	0.109	False		ENSG00000077498	ENSG00000077498	HGNC:12442													
TYRP1	gene	TYRP1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Albinism, oculocutaneous, type III, 203290 (3)						False	3	0;0;0	0.109	False		ENSG00000107165	ENSG00000107165	HGNC:12450													
UBA1	gene	UBA1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	X-LINKED: hemizygous mutation in males, biallelic mutations in females	Spinal muscular atrophy, X-linked 2, infantile, 301830 (3)						False	3	0;0;0	0.109	False		ENSG00000130985	ENSG00000130985	HGNC:12469													
UBA5	gene	UBA5	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Epileptic encephalopathy, early infantile, 44, 617132 (3), Autosomal recessive						False	3	0;0;0	0.109	False		ENSG00000081307	ENSG00000081307	HGNC:23230													
UBE2A	gene	UBE2A	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	X-LINKED: hemizygous mutation in males, biallelic mutations in females	Mental retardation, X-linked syndromic, Nascimento-type, 300860 (3)						False	3	0;0;0	0.109	False		ENSG00000077721	ENSG00000077721	HGNC:12472													
UBE2T	gene	UBE2T	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Fanconi anemia, complementation group T, 616435 (3)						False	3	0;0;0	0.109	False		ENSG00000077152	ENSG00000077152	HGNC:25009													
UBE3B	gene	UBE3B	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Kaufman oculocerebrofacial syndrome, 244450 (3)						False	3	0;0;0	0.109	False		ENSG00000151148	ENSG00000151148	HGNC:13478													
UBR1	gene	UBR1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Johanson-Blizzard syndrome, 243800 (3)						False	3	0;0;0	0.109	False		ENSG00000159459	ENSG00000159459	HGNC:16808													
UFM1	gene	UFM1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Leukodystrophy, hypomyelinating, 14, 617899 (3), Autosomal recessive						False	3	0;0;0	0.109	False		ENSG00000120686	ENSG00000120686	HGNC:20597													
UGT1A1	gene	UGT1A1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Crigler-Najjar syndrome, type I, 218800 (3)						False	3	0;0;0	0.109	False		ENSG00000241635	ENSG00000241635	HGNC:12530													
UMPS	gene	UMPS	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Orotic aciduria, 258900 (3)						False	3	0;0;0	0.109	False		ENSG00000114491	ENSG00000114491	HGNC:12563													
UNC13D	gene	UNC13D	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Hemophagocytic lymphohistiocytosis, familial, 3, 608898 (3)						False	3	0;0;0	0.109	False		ENSG00000092929	ENSG00000092929	HGNC:23147													
UNC80	gene	UNC80	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Hypotonia, infantile, with psychomotor retardation and characteristic facies 2, 616801 (3), Autosomal recessive						False	3	0;0;0	0.109	False		ENSG00000144406	ENSG00000144406	HGNC:26582													
UPF3B	gene	UPF3B	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	X-LINKED: hemizygous mutation in males, biallelic mutations in females	Mental retardation, X-linked, syndromic 14, 300676 (3)						False	3	0;0;0	0.109	False		ENSG00000125351	ENSG00000125351	HGNC:20439													
UQCRQ	gene	UQCRQ	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Mitochondrial complex III deficiency, nuclear type 4, 615159 (3)						False	3	0;0;100	0.109	False		ENSG00000164405	ENSG00000164405	HGNC:29594													
UROS	gene	UROS	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Porphyria, congenital erythropoietic, 263700 (3)						False	3	0;0;0	0.109	False		ENSG00000188690	ENSG00000188690	HGNC:12592													
USB1	gene	USB1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Poikiloderma with neutropenia, 604173 (3)						False	3	0;0;0	0.109	False		ENSG00000103005	ENSG00000103005	HGNC:25792													
USH1C	gene	USH1C	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Usher syndrome, type 1C, 276904 (3)						False	3	0;0;0	0.109	False		ENSG00000006611	ENSG00000006611	HGNC:12597													
USH1G	gene	USH1G	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Usher syndrome, type 1G, 606943 (3)						False	3	0;0;0	0.109	False		ENSG00000182040	ENSG00000182040	HGNC:16356													
USH2A	gene	USH2A	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Usher syndrome, type 2A, 276901 (3)						False	3	0;0;0	0.109	False		ENSG00000042781	ENSG00000042781	HGNC:12601													
USP9X	gene	USP9X	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	X-LINKED: hemizygous mutation in males, biallelic mutations in females	Mental retardation, X-linked 99, 300919 (3)						False	3	0;0;0	0.109	False		ENSG00000124486	ENSG00000124486	HGNC:12632													
VARS	gene	VARS	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Neurodevelopmental disorder with microcephaly, seizures, and cortical atrophy, 617802 (3), Autosomal recessive						False	3	0;0;0	0.109	False		ENSG00000204394	ENSG00000204394	HGNC:12651													
VARS2	gene	VARS2	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Combined oxidative phosphorylation deficiency 20, 615917 (3)						False	3	0;0;0	0.109	False		ENSG00000137411	ENSG00000137411	HGNC:21642													
VIPAS39	gene	VIPAS39	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Arthrogryposis, renal dysfunction, and cholestasis 2, 613404 (3)						False	3	0;0;0	0.109	False		ENSG00000151445	ENSG00000151445	HGNC:20347													
VKORC1	gene	VKORC1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Vitamin K-dependent clotting factors, combined deficiency of, 2, 607473 (3)						False	3	0;0;0	0.109	False		ENSG00000167397	ENSG00000167397	HGNC:23663													
VLDLR	gene	VLDLR	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Cerebellar hypoplasia and mental retardation with or without quadrupedal locomotion 1, 224050 (3)						False	3	0;0;0	0.109	False		ENSG00000147852	ENSG00000147852	HGNC:12698													
VMA21	gene	VMA21	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	X-LINKED: hemizygous mutation in males, biallelic mutations in females	Myopathy, X-linked, with excessive autophagy, 310440 (3), X-linked recessive						False	3	0;0;0	0.109	False		ENSG00000160131	ENSG00000160131	HGNC:22082													
VPS11	gene	VPS11	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Leukodystrophy, hypomyelinating, 12, 616683 (3), Autosomal recessive						False	3	0;0;0	0.109	False		ENSG00000160695	ENSG00000160695	HGNC:14583													
VPS13A	gene	VPS13A	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Choreoacanthocytosis, 200150 (3)						False	3	0;0;0	0.109	False		ENSG00000197969	ENSG00000197969	HGNC:1908													
VPS13B	gene	VPS13B	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Cohen syndrome, 216550 (3)						False	3	0;0;0	0.109	False		ENSG00000132549	ENSG00000132549	HGNC:2183													
VPS33B	gene	VPS33B	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Arthrogryposis, renal dysfunction, and cholestasis 1, 208085 (3)						False	3	0;0;0	0.109	False		ENSG00000184056	ENSG00000184056	HGNC:12712													
VPS37A	gene	VPS37A	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Spastic paraplegia 53, autosomal recessive, 614898 (3)						False	3	0;50;50	0.109	False		ENSG00000155975	ENSG00000155975	HGNC:24928													
VPS45	gene	VPS45	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Neutropenia, severe congenital, 5, autosomal recessive, 615285 (3)						False	3	0;0;0	0.109	False		ENSG00000136631	ENSG00000136631	HGNC:14579													
VPS53	gene	VPS53	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Pontocerebellar hypoplasia, type 2E, 615851 (3)						False	3	0;0;0	0.109	False		ENSG00000141252	ENSG00000141252	HGNC:25608													
VRK1	gene	VRK1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Pontocerebellar hypoplasia type 1A, 607596 (3)						False	3	0;0;0	0.109	False		ENSG00000100749	ENSG00000100749	HGNC:12718													
VSX2	gene	VSX2	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Microphthalmia with coloboma 3, 610092 (3)						False	3	0;0;0	0.109	False		ENSG00000119614	ENSG00000119614	HGNC:1975													
VWF	gene	VWF	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	von Willebrand disease, types 2A, 2B, 2M, and 2N, 613554 (3)						False	3	0;0;0	0.109	False		ENSG00000110799	ENSG00000110799	HGNC:12726													
WARS2	gene	WARS2	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Neurodevelopmental disorder, mitochondrial, with abnormal movements and lactic acidosis, with or without seizures, 617710 (3), Autosomal recessive						False	3	0;0;0	0.109	False		ENSG00000116874	ENSG00000116874	HGNC:12730													
WAS	gene	WAS	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	X-LINKED: hemizygous mutation in males, biallelic mutations in females	Wiskott-Aldrich syndrome, 301000 (3)						False	3	0;0;0	0.109	False		ENSG00000015285	ENSG00000015285	HGNC:12731													
WDR19	gene	WDR19	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Senior-Loken syndrome 8, 616307 (3)						False	3	0;0;0	0.109	False		ENSG00000157796	ENSG00000157796	HGNC:18340													
WDR34	gene	WDR34	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Short-rib thoracic dysplasia 11 with or without polydactyly, 615633 (3)						False	3	0;0;0	0.109	False		ENSG00000119333	ENSG00000119333	HGNC:28296													
WDR35	gene	WDR35	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Short-rib thoracic dysplasia 7 with or without polydactyly, 614091 (3)						False	3	0;0;0	0.109	False		ENSG00000118965	ENSG00000118965	HGNC:29250													
WDR45B	gene	WDR45B	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Neurodevelopmental disorder with spastic quadriplegia and brain abnormalities with or without seizures, 617977 (3), Autosomal recessive						False	3	0;0;0	0.109	False		ENSG00000141580	ENSG00000141580	HGNC:25072													
WDR60	gene	WDR60	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Short-rib thoracic dysplasia 8 with or without polydactyly, 615503 (3)						False	3	0;0;0	0.109	False		ENSG00000126870	ENSG00000126870	HGNC:21862													
WDR62	gene	WDR62	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Microcephaly 2, primary, autosomal recessive, with or without cortical malformations, 604317 (3)						False	3	0;0;0	0.109	False		ENSG00000075702	ENSG00000075702	HGNC:24502													
WDR73	gene	WDR73	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Galloway-Mowat syndrome, 251300 (3)						False	3	0;0;0	0.109	False		ENSG00000177082	ENSG00000177082	HGNC:25928													
WDR81	gene	WDR81	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Cerebellar ataxia, mental retardation, and dysequilibrium syndrome 2, 610185 (3)						False	3	0;0;0	0.109	False		ENSG00000167716	ENSG00000167716	HGNC:26600													
WFS1	gene	WFS1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Wolfram syndrome, 222300 (3)						False	3	0;0;0	0.109	False		ENSG00000109501	ENSG00000109501	HGNC:12762													
WHRN	gene	WHRN	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Usher syndrome, type 2D, 611383 (3)						False	3	0;0;0	0.109	False		ENSG00000095397	ENSG00000095397	HGNC:16361													
WISP3	gene	WISP3	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Arthropathy, progressive pseudorheumatoid, of childhood, 208230 (3)						False	3	0;0;0	0.109	True		ENSG00000112761	ENSG00000112761	HGNC:12771													
WNK1	gene	WNK1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Neuropathy, hereditary sensory and autonomic, type II, 201300 (3)						False	3	0;0;0	0.109	False		ENSG00000060237	ENSG00000060237	HGNC:14540													
WNT1	gene	WNT1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Osteogenesis imperfecta, type XV, 615220 (3)						False	3	0;0;0	0.109	False		ENSG00000125084	ENSG00000125084	HGNC:12774													
WNT10B	gene	WNT10B	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Split-hand/foot malformation 6, 225300 (3)						False	3	0;0;0	0.109	False		ENSG00000169884	ENSG00000169884	HGNC:12775													
WNT7A	gene	WNT7A	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Ulna and fibula, absence of, with severe limb deficiency, 276820 (3)						False	3	0;0;0	0.109	False		ENSG00000154764	ENSG00000154764	HGNC:12786													
WRAP53	gene	WRAP53	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Dyskeratosis congenita, autosomal recessive 3, 613988 (3)						False	3	0;0;0	0.109	False		ENSG00000141499	ENSG00000141499	HGNC:25522													
WRN	gene	WRN	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Werner syndrome, 277700 (3)						False	3	0;0;0	0.109	False		ENSG00000165392	ENSG00000165392	HGNC:12791													
WWOX	gene	WWOX	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Epileptic encephalopathy, early infantile, 28, 616211 (3)						False	3	0;0;0	0.109	False		ENSG00000186153	ENSG00000186153	HGNC:12799													
XIAP	gene	XIAP	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	X-LINKED: hemizygous mutation in males, biallelic mutations in females	Lymphoproliferative syndrome, X-linked, 2, 300635 (3)						False	3	0;0;0	0.109	False		ENSG00000101966	ENSG00000101966	HGNC:592													
XPA	gene	XPA	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Xeroderma pigmentosum, group A, 278700 (3)						False	3	0;0;0	0.109	False		ENSG00000136936	ENSG00000136936	HGNC:12814													
XPC	gene	XPC	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Xeroderma pigmentosum, group C, 278720 (3)						False	3	0;0;0	0.109	False		ENSG00000154767	ENSG00000154767	HGNC:12816													
XRCC4	gene	XRCC4	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Short stature, microcephaly, and endocrine dysfunction, 616541 (3), Autosomal recessive						False	3	0;0;0	0.109	False		ENSG00000152422	ENSG00000152422	HGNC:12831													
XYLT1	gene	XYLT1	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Desbuquois dysplasia 2, 615777 (3)						False	3	0;0;0	0.109	False		ENSG00000103489	ENSG00000103489	HGNC:15516													
XYLT2	gene	XYLT2	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Spondyloocular syndrome, 605822 (3), Autosomal recessive						False	3	0;0;0	0.109	False		ENSG00000015532	ENSG00000015532	HGNC:15517													
YARS2	gene	YARS2	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Myopathy, lactic acidosis, and sideroblastic anemia 2, 613561 (3)						False	3	0;0;0	0.109	False		ENSG00000139131	ENSG00000139131	HGNC:24249													
ZAP70	gene	ZAP70	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Selective T-cell defect, 269840 (3)						False	3	0;0;0	0.109	False		ENSG00000115085	ENSG00000115085	HGNC:12858													
ZBTB24	gene	ZBTB24	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Immunodeficiency-centromeric instability-facial anomalies syndrome-2, 614069 (3)						False	3	0;0;0	0.109	False		ENSG00000112365	ENSG00000112365	HGNC:21143													
ZC4H2	gene	ZC4H2	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	X-LINKED: hemizygous mutation in males, biallelic mutations in females	Wieacker-Wolff syndrome, 314580 (3)						False	3	0;0;0	0.109	False		ENSG00000126970	ENSG00000126970	HGNC:24931													
ZDHHC9	gene	ZDHHC9	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	X-LINKED: hemizygous mutation in males, biallelic mutations in females	Mental retardation, X-linked syndromic, Raymond type, 300799 (3)						False	3	0;0;0	0.109	False		ENSG00000188706	ENSG00000188706	HGNC:18475													
ZFYVE26	gene	ZFYVE26	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Spastic paraplegia 15, autosomal recessive, 270700 (3)						False	3	0;0;0	0.109	False		ENSG00000072121	ENSG00000072121	HGNC:20761													
ZIC3	gene	ZIC3	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	X-LINKED: hemizygous mutation in males, biallelic mutations in females	Congenital heart defects, nonsyndromic, 1, X-linked, 306955 (3)						False	3	0;0;0	0.109	False		ENSG00000156925	ENSG00000156925	HGNC:12874													
ZMPSTE24	gene	ZMPSTE24	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Restrictive dermopathy, lethal, 275210 (3)						False	3	0;0;0	0.109	False		ENSG00000084073	ENSG00000084073	HGNC:12877													
ZMYND10	gene	ZMYND10	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Ciliary dyskinesia, primary, 22, 615444 (3)						False	3	0;0;0	0.109	False		ENSG00000004838	ENSG00000004838	HGNC:19412													
ZNF335	gene	ZNF335	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Microcephaly 10, primary, autosomal recessive						False	3	0;0;0	0.109	False		ENSG00000198026	ENSG00000198026	HGNC:15807													
ZNF711	gene	ZNF711	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	X-LINKED: hemizygous mutation in males, biallelic mutations in females	Mental retardation, X-linked 97, 300803 (3)						False	3	0;0;0	0.109	False		ENSG00000147180	ENSG00000147180	HGNC:13128													
ZNHIT3	gene	ZNHIT3	Expert Review Green;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	PEHO syndrome, 260565 (3), Autosomal recessive						False	3	0;0;0	0.109	False		ENSG00000108278	ENSG00000273611	HGNC:12309													
B9D1	gene	B9D1	Expert Review Amber;Literature	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Meckel syndrome 9, MIM# 614209;Joubert syndrome 27, MIM# 617120				24886560;21493627;25920555		False	2	0;0;0	0.109	True		ENSG00000108641	ENSG00000108641	HGNC:24123													
COL2A1	gene	COL2A1	Expert Review Amber;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	Spondyloperipheral dysplasia, MIM #271700				31755234;32896647		False	2	0;100;0	0.109	True		ENSG00000139219	ENSG00000139219	HGNC:2200													
DYNC1I2	gene	DYNC1I2	Expert Review;Expert Review Amber	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	"Neurodevelopmental disorder with microcephaly and structural brain anomalies	, MIM#618492"				31079899		False	2	50;0;50	0.109	True		ENSG00000077380	ENSG00000077380	HGNC:2964													
ERBB3	gene	ERBB3	Expert Review Amber;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Lethal congenital contractural syndrome 2, 607598 (3)						False	2	50;50;0	0.109	True		ENSG00000065361	ENSG00000065361	HGNC:3431													
KCNE1	gene	KCNE1	Expert Review Amber;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Jervell and Lange-Nielsen syndrome 2, 612347 (3)						False	2	50;50;0	0.109	False		ENSG00000180509	ENSG00000180509	HGNC:6240													
MBTPS1	gene	MBTPS1	Expert Review;Expert Review Amber;Literature	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	?Spondyloepiphyseal dysplasia, Kondo-Fu type, MIM #618392				32857899;32420688;30046013		False	2	0;100;0	0.109	True		ENSG00000140943	ENSG00000140943	HGNC:15456													
MOGS	gene	MOGS	Expert Review;Expert Review Amber	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Congenital disorder of glycosylation, type IIb, MIM# 606056				31925597;30587846;33058492		False	2	100;0;0	0.109	True		ENSG00000115275	ENSG00000115275	HGNC:24862													
NTNG2	gene	NTNG2	Expert Review;Expert Review Amber	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Neurodevelopmental disorder with behavioral abnormalities, absent speech, and hypotonia, MIM# 618718				31668703;31692205		False	2	100;0;0	0.109	True		ENSG00000196358	ENSG00000196358	HGNC:14288													
POLA1	gene	POLA1	Expert Review Amber;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	X-LINKED: hemizygous mutation in males, biallelic mutations in females	Pigmentary disorder, reticulate, with systemic manifestations, X-linked, MIM#301220;Van Esch-O'Driscoll syndrome, MIM #301030						False	2	0;100;0	0.109	True		ENSG00000101868	ENSG00000101868	HGNC:9173													
RPL10	gene	RPL10	Expert Review Amber;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	X-LINKED: hemizygous mutation in males, biallelic mutations in females	Mental retardation, X-linked, syndromic, 35 (MIM#300998)						False	2	0;100;0	0.109	True		ENSG00000147403	ENSG00000147403	HGNC:10298													
TMEM94	gene	TMEM94	Expert list;Expert Review Amber	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Intellectual developmental disorder with cardiac defects and dysmorphic facies, MIM#618316				30526868		False	2	50;50;0	0.109	True		ENSG00000177728	ENSG00000177728	HGNC:28983													
TRAC	gene	TRAC	Expert Review Amber;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Immunodeficiency 7, TCR-alpha/beta deficient, 615387 (3)						False	2	0;100;0	0.109	True		ENSG00000229164	ENSG00000277734	HGNC:12029													
XPNPEP3	gene	XPNPEP3	Expert Review Amber;Mackenzie's Mission	Mackenzie's Mission_Reproductive Carrier Screening		Screening	BIALLELIC, autosomal or pseudoautosomal	Nephronophthisis-like nephropathy 1, 613159 (3)						False	2	0;100;0	0.109	True		ENSG00000196236	ENSG00000196236	HGNC:28052