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
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	0.433	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	0;100;0	0.433	True		ENSG00000162063	ENSG00000162063	HGNC:1591													
DNAJC7	gene	DNAJC7	Expert Review Amber;Literature	Incidentalome			MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	amyotrophic lateral sclerosis				31768050;40802071		False	2	0;100;0	0.433	True		ENSG00000168259	ENSG00000168259	HGNC:12392													
GLT8D1	gene	GLT8D1	ClinGen;Expert Review Amber	Incidentalome			MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	amyotrophic lateral sclerosis MONDO:0004976				30811981;35525134;34746377;33714647;31653410;35873773;33581933		False	2	0;100;0	0.433	True		ENSG00000016864	ENSG00000016864	HGNC:24870													
LGALSL	gene	LGALSL	ClinGen;Expert Review Amber	Incidentalome			Unknown	"Amyotrophic lateral sclerosis	MONDO:0004976"				30940688		False	2	0;100;0	0.433	True		ENSG00000119862	ENSG00000119862	HGNC:25012													
PCDHA9	gene	PCDHA9	Expert Review Amber;Literature	Incidentalome			BIALLELIC, autosomal or pseudoautosomal	amyotrophic lateral sclerosis MONDO:0004976				38467605		False	2	0;100;0	0.433	True		ENSG00000204961	ENSG00000204961	HGNC:8675													
RBM12	gene	RBM12	Expert Review Amber;Victorian Clinical Genetics Services	Incidentalome			Unknown	Schizophrenia 19 (MIM#617629)						False	2	0;100;0	0.433	True		ENSG00000244462	ENSG00000244462	HGNC:9898													
SORL1	gene	SORL1	Expert Review Amber;Victorian Clinical Genetics Services	Incidentalome			MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Alzheimer disease, MONDO:0004975, SORL1-related				27026413;39226352;40182695		False	2	0;50;50	0.433	True		ENSG00000137642	ENSG00000137642	HGNC:11185													
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	0.433	True		ENSG00000184402	ENSG00000184402	HGNC:15592													
TAF15	gene	TAF15	ClinGen;Expert Review Amber	Incidentalome			MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	amyotrophic lateral sclerosis MONDO:0004976;frontotemporal dementia MONDO:0017276				28889094;21438137;22065782;27810362;28889094		False	2	0;100;0	0.433	True		ENSG00000172660	ENSG00000270647	HGNC:11547													
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	0.433	True		ENSG00000127824	ENSG00000127824	HGNC:12407													
UBQLN4	gene	UBQLN4	Expert Review;Expert Review Amber	Incidentalome			MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	amyotrophic lateral sclerosis MONDO:0004976				28463112;30804504		False	2	0;100;0	0.433	True		ENSG00000160803	ENSG00000160803	HGNC:1237													
UQCRC1	gene	UQCRC1	Expert Review Amber;Literature	Incidentalome			MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Parkinsonism with polyneuropathy, MIM# 619279				33141179;33248804		False	2	50;50;0	0.433	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	0.433	True		ENSG00000165238	ENSG00000165238	HGNC:14542