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
KCNH2	gene	KCNH2	Expert Review Green;Victorian Clinical Genetics Services	Short QT syndrome		Cardiovascular disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Short QT syndrome			Shortened QT interval;HP:0012232	34557911		False	3	100;0;0	1.7	True	Other	ENSG00000055118	ENSG00000055118	HGNC:6251													
KCNJ2	gene	KCNJ2	Expert Review Green;Victorian Clinical Genetics Services	Short QT syndrome		Cardiovascular disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Short QT syndrome			Shortened QT interval;HP:0012232	34557911		False	3	100;0;0	1.7	True	Other	ENSG00000123700	ENSG00000123700	HGNC:6263													
KCNQ1	gene	KCNQ1	Expert Review Green;Victorian Clinical Genetics Services	Short QT syndrome		Cardiovascular disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Short QT syndrome 1;bradycardia;atrial fibrillation			Shortened QT interval;HP:0012232	34557911		False	3	100;0;0	1.7	True		ENSG00000053918	ENSG00000053918	HGNC:6294													
SLC4A3	gene	SLC4A3	Expert Review;Expert Review Green	Short QT syndrome		Cardiovascular disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Short QT syndrome 7, MIM#620231			Shortened QT interval;HP:0012232	29167417;34557911;36806574		False	3	67;33;0	1.7	True		ENSG00000114923	ENSG00000114923	HGNC:11029