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
BVES	gene	BVES	Expert Review Red;Literature	Arrhythmogenic Cardiomyopathy		Cardiovascular disorders	BIALLELIC, autosomal or pseudoautosomal	Muscular dystrophy, limb-girdle, autosomal recessive 25 616812			Arrhythmia;HP:0011675;Cardiomyopathy;HP:0001638	26642364;31119192		False	1	0;100;0	0.68	True		ENSG00000112276	ENSG00000112276	HGNC:1152													
RYR2	gene	RYR2	Expert Review Red;Victorian Clinical Genetics Services	Arrhythmogenic Cardiomyopathy		Cardiovascular disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Arrhythmogenic right ventricular dysplasia 2, MIM# 600996			Arrhythmia;HP:0011675;Cardiomyopathy;HP:0001638	11159936;25041964;29543670		False	1	0;0;100	0.68	True		ENSG00000198626	ENSG00000198626	HGNC:10484													
TGFB3	gene	TGFB3	Expert Review Red;Victorian Clinical Genetics Services	Arrhythmogenic Cardiomyopathy		Cardiovascular disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Arrhythmogenic right ventricular dysplasia 1, MIM# 107970			Arrhythmia;HP:0011675;Cardiomyopathy;HP:0001638	15639475		False	1	0;0;100	0.68	True		ENSG00000119699	ENSG00000119699	HGNC:11769