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
CACNA1S	gene	CACNA1S	Expert list;Expert Review Green	Pharmacogenomics_Paediatric		Screening	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	"{Malignant hyperthermia susceptibility 5}, MIM#	601887"				30499100		False	3	100;0;0	0.50	True		ENSG00000081248	ENSG00000081248	HGNC:1397													
CYP2C19	gene	CYP2C19	Expert Review Green;Other	Pharmacogenomics_Paediatric		Screening	Other	Voriconazole				27981572;26616742;31549386		False	3	100;0;0	0.50	True		ENSG00000165841	ENSG00000165841	HGNC:2621													
CYP2C9	gene	CYP2C9	Expert list;Expert Review Green	Pharmacogenomics_Paediatric		Screening	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	"Warfarin sensitivity, MIM#	122700;Phenytoin"				25099164;21900891;28198005		False	3	100;0;0	0.50	True		ENSG00000138109	ENSG00000138109	HGNC:2623													
CYP2D6	gene	CYP2D6	Expert Review Green;Other	Pharmacogenomics_Paediatric		Screening	Other	Codeine, tramadol, oxycodone				18406467;24458010		False	3	100;0;0	0.50	True		ENSG00000100197	ENSG00000100197	HGNC:2625													
CYP3A5	gene	CYP3A5	Expert list;Expert Review Green	Pharmacogenomics_Paediatric		Screening	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Tacrolimus				25801146;25201288		False	3	100;0;0	0.50	True		ENSG00000106258	ENSG00000106258	HGNC:2638													
G6PD	gene	G6PD	Expert list;Expert Review Green	Pharmacogenomics_Paediatric		Screening	X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)	"Haemolytic anemia, G6PD deficient (favism), MIM#	300908"						False	3	100;0;0	0.50	True		ENSG00000160211	ENSG00000160211	HGNC:4057													
HLA-A	gene	HLA-A	Expert list;Expert Review Green	Pharmacogenomics_Paediatric		Screening	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Carbamazepine						False	3	100;0;0	0.50	True		ENSG00000206503	ENSG00000206503	HGNC:4931													
HLA-B	gene	HLA-B	Expert list;Expert Review Green	Pharmacogenomics_Paediatric		Screening	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Carbamazepine;Oxcarbamazepine;Phenytoin				25099164;23695185;29392710;26094938		False	3	100;0;0	0.50	True		ENSG00000234745	ENSG00000234745	HGNC:4932													
MT-RNR1	gene	MT-RNR1	Expert list;Expert Review Green	Pharmacogenomics_Paediatric		Screening	MITOCHONDRIAL	Gentamicin toxicity						False	3	100;0;0	0.50	True		ENSG00000211459	ENSG00000211459	HGNC:7470													
NUDT15	gene	NUDT15	Expert list;Expert Review Green	Pharmacogenomics_Paediatric		Screening	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	"{Thiopurines, poor metabolism of, 2}	616903;Azathioprine;Mercaptopurine"				21270794;23422873;30447069		False	3	100;0;0	0.50	True		ENSG00000136159	ENSG00000136159	HGNC:23063													
RYR1	gene	RYR1	Expert list;Expert Review Green	Pharmacogenomics_Paediatric		Screening	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	"{Malignant hyperthermia susceptibility 1}	145600"				30499100		False	3	100;0;0	0.50	True		ENSG00000196218	ENSG00000196218	HGNC:10483													
TPMT	gene	TPMT	Expert list;Expert Review Green	Pharmacogenomics_Paediatric		Screening	BIALLELIC, autosomal or pseudoautosomal	"{Thiopurines, poor metabolism of, 1}, MIM#	610460;Azathioprine;Mercaptopurine;Thioguanines"				21270794;23422873;30447069		False	3	100;0;0	0.50	True		ENSG00000137364	ENSG00000137364	HGNC:12014													
VKORC1	gene	VKORC1	Expert list;Expert Review Green	Pharmacogenomics_Paediatric		Screening	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	"Warfarin resistance, MIM#	122700"				21900891;28198005		False	3	100;0;0	0.50	True		ENSG00000167397	ENSG00000167397	HGNC:23663													
DPYD	gene	DPYD	Expert Review Amber;Other	Pharmacogenomics_Paediatric		Screening	Other	Fluoropyrimidine				29152729		False	2	0;100;0	0.50	True	Other	ENSG00000188641	ENSG00000188641	HGNC:3012													
POLG	gene	POLG	Expert Review Amber;Other	Pharmacogenomics_Paediatric		Screening	BIALLELIC, autosomal or pseudoautosomal	Alpers syndrome				20138553		False	2	0;100;0	0.50	True		ENSG00000140521	ENSG00000140521	HGNC:9179