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
ATP1A3	gene	ATP1A3	Expert Review;Expert Review Green	Auditory Neuropathy Spectrum Disorde	Non-syndromic hearing loss	Hearing and ear disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	601338;614820				PMID: 25447930 		False	3	100;0;0	1.10	True	Other - please provide details in the comments	ENSG00000105409	ENSG00000105409	HGNC:801													
DFNB59	gene	DFNB59	Expert Review;Expert Review Green	Auditory Neuropathy Spectrum Disorde	Non-syndromic hearing loss	Hearing and ear disorders	BIALLELIC, autosomal or pseudoautosomal	610219				16804542		False	3	100;0;0	1.10	True		ENSG00000204311	ENSG00000204311	HGNC:29502													
OPA1	gene	OPA1	Eligibility statement prior genetic testing;Expert Review Green	Auditory Neuropathy Spectrum Disorde	Non-syndromic hearing loss	Hearing and ear disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Optic atrophy 1, OMIM:165500;Optic atrophy plus syndrome, OMIM:125250				11017079		False	3	100;0;0	1.10	True		ENSG00000198836	ENSG00000198836	HGNC:8140													
OTOF	gene	OTOF	Expert Review Green;Radboud University Medical Center, Nijmegen	Auditory Neuropathy Spectrum Disorde	Non-syndromic hearing loss	Hearing and ear disorders	BIALLELIC, autosomal or pseudoautosomal	601071				10192385		False	3	100;0;0	1.10	True		ENSG00000115155	ENSG00000115155	HGNC:8515													
DIAPH3	gene	DIAPH3	Expert Review Amber;Radboud University Medical Center, Nijmegen	Auditory Neuropathy Spectrum Disorde	Non-syndromic hearing loss	Hearing and ear disorders	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	Auditory neuropathy, autosomal dominant, 1, 609129				20624953;27658576		False	2	0;0;100	1.10	True		ENSG00000139734	ENSG00000139734	HGNC:15480