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
GYG1	gene	GYG1	Expert Review;Expert Review Amber	Hypertrophic cardiomyopathy_HCM		Cardiovascular disorders	BIALLELIC, autosomal or pseudoautosomal	Hypertrophic Cardiomyopathy			Hypertrophic cardiomyopathy;HP:0001639	27718144;20357282;31628455		False	2	0;100;0	1.0	True		ENSG00000163754	ENSG00000163754	HGNC:4699													
JPH2	gene	JPH2	Expert Review Amber;Victorian Clinical Genetics Services	Hypertrophic cardiomyopathy_HCM		Cardiovascular disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Cardiomyopathy, hypertrophic, MIM#613873			Hypertrophic cardiomyopathy;HP:0001639	30681346;17509612;23973696;26869393;28393127;30235249		False	2	0;100;0	1.0	True		ENSG00000149596	ENSG00000149596	HGNC:14202													
NEBL	gene	NEBL	Expert Review Amber;Literature	Hypertrophic cardiomyopathy_HCM		Cardiovascular disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Hypertrophic cardiomyopathy;dilated cardiomyopathy			Hypertrophic cardiomyopathy;HP:0001639	27186169		False	2	100;0;0	1.0	True		ENSG00000078114	ENSG00000078114	HGNC:16932													
RPS6KB1	gene	RPS6KB1	Expert Review Amber;Literature	Hypertrophic cardiomyopathy_HCM		Cardiovascular disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Hypertrophic cardiomyopathy, MONDO:0005045, RPS6KB1-related			Hypertrophic cardiomyopathy;HP:0001639	34916228		False	2	100;0;0	1.0	True		ENSG00000108443	ENSG00000108443	HGNC:10436													
TTN	gene	TTN	Expert Review Amber;Victorian Clinical Genetics Services	Hypertrophic cardiomyopathy_HCM		Cardiovascular disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Hypertrophic cardiomyopathy			Hypertrophic cardiomyopathy;HP:0001639	27625337;31628103		False	2	0;100;0	1.0	True		ENSG00000155657	ENSG00000155657	HGNC:12403													
TULP3	gene	TULP3	Expert Review Amber;Literature	Hypertrophic cardiomyopathy_HCM		Cardiovascular disorders	BIALLELIC, autosomal or pseudoautosomal	Hepatorenocardiac degenerative fibrosis, MIM# 619902			Hypertrophic cardiomyopathy;HP:0001639	PMID: 35397207		False	2	100;0;0	1.0	True		ENSG00000078246	ENSG00000078246	HGNC:12425