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
ATAD3A	gene	ATAD3A	Expert Review Amber;Literature	Hypertrophic cardiomyopathy		Cardiology	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	Harel-Yoon syndrome, OMIM:617183				27640307;28652416;28158749;31727539		False	2	0;100;0	5.29	False		ENSG00000197785	ENSG00000197785	HGNC:25567													
GYG1	gene	GYG1	Expert Review Amber;Literature	Hypertrophic cardiomyopathy		Cardiology	BIALLELIC, autosomal or pseudoautosomal	?Glycogen storage disease XV, OMIM:613507;hypertrophic cardiomyopathy, MONDO:0005045				27718144;20357282;31628455		False	2	0;100;0	5.29	False		ENSG00000163754	ENSG00000163754	HGNC:4699													
JPH2	gene	JPH2	Emory Genetics Laboratory;Expert list;Expert Review Amber;London South GLH;NHS GMS;Radboud University Medical Center, Nijmegen;South West GLH	Hypertrophic cardiomyopathy		Cardiology	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Cardiomyopathy, hypertrophic, 17, OMIM:613873				28393127;17509612;17476457;30681346;23973696;26869393;28393127;30235249		False	2	22;78;0	5.29	False		ENSG00000149596	ENSG00000149596	HGNC:14202													
MT-TI	gene	MT-TI	Expert Review Amber;NHS GMS;Wessex and West Midlands GLH	Hypertrophic cardiomyopathy		Cardiology	MITOCHONDRIAL	familial hypertrophic cardiomyopathy, MONDO:0024573;familial dilated cardiomyopathy, MONDO:0016333				12767666;21945886;23332932;29481798;30025578;39639347		False	2	40;60;0	5.29	True		ENSG00000210100	ENSG00000210100	HGNC:7488													
MYLK2	gene	MYLK2	Expert list;Illumina TruGenome Clinical Sequencing Services;London South GLH;North West GLH;Radboud University Medical Center, Nijmegen;South West GLH	Hypertrophic cardiomyopathy		Cardiology	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Cardiomyopathy, hypertrophic, 1, digenic (192600);Cardiomyopathy, hypertrophic, midventricular, digenic, 				27532257;28369730;30681346		False	2	0;100;0	5.29	False		ENSG00000101306	ENSG00000101306	HGNC:16243													
MYPN	gene	MYPN	Emory Genetics Laboratory;Expert list;London South GLH;Radboud University Medical Center, Nijmegen;South West GLH	Hypertrophic cardiomyopathy		Cardiology	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Cardiomypathy, familial hypertrophic, 22, 						False	2	0;75;25	5.29	False		ENSG00000138347	ENSG00000138347	HGNC:23246													
RPS6KB1	gene	RPS6KB1	Expert Review Amber;Literature	Hypertrophic cardiomyopathy		Cardiology	MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	Hypertrophic cardiomyopathy				34916228		False	2	100;0;0	5.29	False		ENSG00000108443	ENSG00000108443	HGNC:10436													
SVIL	gene	SVIL	Expert Review Amber;Literature	Hypertrophic cardiomyopathy		Cardiology	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	hypertrophic cardiomyopathy, MONDO:0005045				39966646;32779703;25633252		False	2	0;100;0	5.29	False		ENSG00000197321	ENSG00000197321	HGNC:11480													
TULP3	gene	TULP3	Expert list;Expert Review Amber	Hypertrophic cardiomyopathy		Cardiology	BIALLELIC, autosomal or pseudoautosomal	Hepatorenocardiac degenerative fibrosis, OMIM:619902				35397207;36460032		False	2	50;0;50	5.29	False		ENSG00000078246	ENSG00000078246	HGNC:12425