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
CAV3	gene	CAV3	Expert Review Amber;Victorian Clinical Genetics Services	Long QT Syndrome		Cardiovascular disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Long QT syndrome 9, MIM# 611818			Prolonged QT interval;HP:0001657	31983240;17060380		False	2	0;100;0	0.61	True		ENSG00000182533	ENSG00000182533	HGNC:1529													
KCNE1	gene	KCNE1	Expert Review Amber;Victorian Clinical Genetics Services	Long QT Syndrome		Cardiovascular disorders	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	Jervell and Lange-Nielsen syndrome 2, MIM# 612347;Long QT syndrome 5, MIM# 613695;Acquired LQTS			Prolonged QT interval;HP:0001657	31983240		False	2	0;100;0	0.61	True		ENSG00000180509	ENSG00000180509	HGNC:6240													
KCNE2	gene	KCNE2	Expert Review Amber;Victorian Clinical Genetics Services	Long QT Syndrome		Cardiovascular disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Long QT syndrome			Prolonged QT interval;HP:0001657	31983240;28794082		False	2	0;100;0	0.61	True		ENSG00000159197	ENSG00000159197	HGNC:6242