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
KCNE2	gene	KCNE2	Emory Genetics Laboratory;Expert list;Expert Review Amber;Illumina TruGenome Clinical Sequencing Services;London South GLH;North West GLH;Radboud University Medical Center, Nijmegen;South West GLH;UKGTN	Long QT syndrome		Cardiology	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Long QT syndrome 6 (613693);Atrial fibrillation, familial, 4 (611493)				19716085;26888179;11468227		False	2	62;38;0	3.12	False		ENSG00000159197	ENSG00000159197	HGNC:6242													
TECRL	gene	TECRL	Expert Review Amber;NHS GMS	Long QT syndrome		Cardiology	BIALLELIC, autosomal or pseudoautosomal	Ventricular tachycardia, catecholaminergic polymorphic, 3, 614021						False	2	0;100;0	3.12	False		ENSG00000205678	ENSG00000205678	HGNC:27365													
TRDN	gene	TRDN	Expert list;Expert Review Amber	Long QT syndrome		Cardiology	BIALLELIC, autosomal or pseudoautosomal	Long QT syndrome				31983240;25922419		False	2	100;0;0	3.12	False		ENSG00000186439	ENSG00000186439	HGNC:12261