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
CACNA2D1	gene	CACNA2D1	Brugada syndrome (Version 1.7);Expert Review Amber;Literature;London South GLH;North West GLH;South West GLH;UKGTN	Short QT syndrome		Cardiology	MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	short qt;Brugada syndrome;aborted sudden death;Short QT syndrome 6				30420954;19862833;16301704		False	2	14;71;14	3.16	True		ENSG00000153956	ENSG00000153956	HGNC:1399													
CACNB2	gene	CACNB2	Brugada syndrome (Version 1.7);Expert Review Amber;Literature;London South GLH;North West GLH;South West GLH;UKGTN	Short QT syndrome		Cardiology	MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	Brugada syndrome 4 (611876);Short QT syndrome 5;brugada syndrome;Brugada syndrome 4 611876;short qt				30420954;19862833;16301704		False	2	14;71;14	3.16	False		ENSG00000165995	ENSG00000165995	HGNC:1402													
SCN5A	gene	SCN5A	Brugada syndrome (Version 1.7);Emory Genetics Laboratory;Expert Review Amber;Literature;Long QT syndrome (Version 1.5);North West GLH;South West GLH	Short QT syndrome		Cardiology	MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	Ventricular fibrillation, familial, 1 (603829);Brugada syndrome 1 (601144);{Sudden infant death syndrome, susceptibility to} (272120);Brugada syndrome 1 601144;Heart block, progressive, type IA (113900);Heart block, nonprogressive (113900);Sick sinus syndrome 1 (608567);Long QT syndrome-3 (603830);Cardiomyopathy, dilated, 1E (601154);Atrial fibrillation, familial, 10 (614022)				16301704;30420954;22490985		False	2	25;25;50	3.16	False		ENSG00000183873	ENSG00000183873	HGNC:10593													
SLC4A3	gene	SLC4A3	Expert Review Amber;Literature;South West GLH;West Midlands, Oxford and Wessex GLH	Short QT syndrome		Cardiology	MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	short QT;ventricular fibrillation;cardiac arrest				29167417;29697308		False	2	20;60;20	3.16	False		ENSG00000114923	ENSG00000114923	HGNC:11029