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
ANK2	gene	ANK2	Expert Review Amber;NHS GMS	Arrhythmogenic right ventricular cardiomyopathy		Cardiology	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted							False	2	0;100;0	3.15	False		ENSG00000145362	ENSG00000145362	HGNC:493													
CDH2	gene	CDH2	Expert list;Expert Review Amber	Arrhythmogenic right ventricular cardiomyopathy		Cardiology	MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	Arrhythmogenic right ventricular dysplasia, familial, 14, 618920				28326674;28280076;24294380		False	2	33;67;0	3.15	False		ENSG00000170558	ENSG00000170558	HGNC:1759													
