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
A2M	gene	A2M	Expert Review Amber;Victorian Clinical Genetics Services	Incidentalome			MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Alzheimer disease, MONDO:0004975						False	2	0;0;100	0.318	True		ENSG00000175899	ENSG00000175899	HGNC:7													
ANG	gene	ANG	Expert Review Amber;Victorian Clinical Genetics Services	Incidentalome			MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Amyotrophic Lateral Sclerosis (MONDO: 0012753;MIM#611895)				17886298;16501576;18087731;20301623;19153377		False	2	50;0;50	0.318	True		ENSG00000214274	ENSG00000214274	HGNC:483													
CCNF	gene	CCNF	Expert list;Expert Review Amber	Incidentalome			MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Frontotemporal dementia and/or amyotrophic lateral sclerosis 5, MIM# 619141				27080313;31577344		False	2	50;50;0	0.318	True		ENSG00000162063	ENSG00000162063	HGNC:1591													
DNAJC7	gene	DNAJC7	Expert Review Amber;Literature	Incidentalome			MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	amyotrophic lateral sclerosis				31768050		False	2	0;100;0	0.318	True		ENSG00000168259	ENSG00000168259	HGNC:12392													
KCNE2	gene	KCNE2	Expert Review Amber;Victorian Clinical Genetics Services	Incidentalome			MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Long QT syndrome 6, MIM# 613693				31983240;28794082;31983240		False	2	0;100;0	0.318	True		ENSG00000159197	ENSG00000159197	HGNC:6242													
RBM12	gene	RBM12	Expert Review Amber;Victorian Clinical Genetics Services	Incidentalome			Unknown							False	2	0;100;0	0.318	True		ENSG00000244462	ENSG00000244462	HGNC:9898													
SS18L1	gene	SS18L1	Expert Review;Expert Review Amber	Incidentalome			MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	amyotrophic lateral sclerosis (MONDO:0004976)				25888396;24360741;23708140;30976389		False	2	0;100;0	0.318	True		ENSG00000184402	ENSG00000184402	HGNC:15592													
TUBA4A	gene	TUBA4A	Expert Review Amber;Royal Melbourne Hospital;Victorian Clinical Genetics Services	Incidentalome			MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Amyotrophic lateral sclerosis 22 with or without frontotemporal dementia, MIM# 616208				28069311;25374358;26675813		False	2	0;100;0	0.318	True		ENSG00000127824	ENSG00000127824	HGNC:12407													
UQCRC1	gene	UQCRC1	Expert Review Amber;Literature	Incidentalome			MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Parkinsonism with polyneuropathy, MIM# 619279				33141179;33248804		False	2	0;100;0	0.318	True		ENSG00000010256	ENSG00000010256	HGNC:12585													
WNK2	gene	WNK2	Expert Review Amber;Literature	Incidentalome			MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Serrated polyposis syndrome				PMID: 36270769		False	2	0;100;0	0.318	True		ENSG00000165238	ENSG00000165238	HGNC:14542