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
CACNA1D	gene	CACNA1D	Expert Review Amber;Literature	Cardiac arrhythmias		Cardiology	BIALLELIC, autosomal or pseudoautosomal	Sinoatrial node dysfunction and deafness, OMIM:614896;sinoatrial node dysfunction and deafness, MONDO:0013960				21131953;30498240;30054272;32747562		False	2	100;0;0	14.21	False		ENSG00000157388	ENSG00000157388	HGNC:1391													
CACNA2D1	gene	CACNA2D1	Expert Review Amber;South West GLH;London South GLH;North West GLH;UKGTN;Brugada syndrome (Version 1.7);Literature	Cardiac arrhythmias		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	14.21	True		ENSG00000153956	ENSG00000153956	HGNC:1399													
CACNB2	gene	CACNB2	South West GLH;London South GLH;North West GLH;Expert Review Amber;UKGTN;Brugada syndrome (Version 1.7);Literature	Cardiac arrhythmias		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	14.21	False		ENSG00000165995	ENSG00000165995	HGNC:1402													
KCNE2	gene	KCNE2	Expert Review Amber;South West GLH;London South GLH;North West GLH;Emory Genetics Laboratory;Expert list;UKGTN;Illumina TruGenome Clinical Sequencing Services;Radboud University Medical Center, Nijmegen	Cardiac arrhythmias		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	14.21	False		ENSG00000159197	ENSG00000159197	HGNC:6242													
SCN5A	gene	SCN5A	South West GLH;North West GLH;Expert Review Amber;Brugada syndrome (Version 1.7);Long QT syndrome (Version 1.5);Emory Genetics Laboratory;Literature	Cardiac arrhythmias		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	14.21	False		ENSG00000183873	ENSG00000183873	HGNC:10593													
SLC4A3	gene	SLC4A3	Expert Review Amber;West Midlands, Oxford and Wessex GLH;South West GLH;Literature	Cardiac arrhythmias		Cardiology	MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	short QT;ventricular fibrillation;cardiac arrest				29167417;29697308		False	2	20;60;20	14.21	False		ENSG00000114923	ENSG00000114923	HGNC:11029													
TANGO2	gene	TANGO2	Expert Review Amber;Expert Review	Cardiac arrhythmias		Cardiology	BIALLELIC, autosomal or pseudoautosomal	Metabolic encephalomyopathic crises, recurrent, with rhabdomyolysis, cardiac arrhythmias, and neurodegeneration, OMIM:616878;recurrent metabolic encephalomyopathic crises-rhabdomyolysis-cardiac arrhythmia-intellectual disability syndrome, MONDO:0018820				26805781;26805782;30245509;31339582;32929747;35568137;40156300		False	2	50;50;0	14.21	False		ENSG00000183597	ENSG00000183597	HGNC:25439													
TECRL	gene	TECRL	Expert Review Amber;NHS GMS	Cardiac arrhythmias		Cardiology	BIALLELIC, autosomal or pseudoautosomal	Ventricular tachycardia, catecholaminergic polymorphic, 3, 614021						False	2	0;100;0	14.21	False		ENSG00000205678	ENSG00000205678	HGNC:27365													
TRDN	gene	TRDN	Expert Review Amber;Expert list	Cardiac arrhythmias		Cardiology	BIALLELIC, autosomal or pseudoautosomal	Long QT syndrome				31983240;25922419		False	2	100;0;0	14.21	False		ENSG00000186439	ENSG00000186439	HGNC:12261