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
CACNA1C	gene	CACNA1C	Brugada syndrome (Version 1.7);Emory Genetics Laboratory;Expert Review Green;Literature;London South GLH;Long QT syndrome (Version 1.5);North West GLH;South West GLH;UKGTN;West Midlands, Oxford and Wessex GLH	Short QT syndrome		Cardiology	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Timothy syndrome, OMIM:601005;Timothy syndrome, MONDO:0010979;Long QT syndrome 8, OMIM:618447;long qt syndrome 8, MONDO:0032756;Brugada syndrome 3, OMIM:611875;Brugada syndrome 3, MONDO:0012742;Short QT;CACNA1C-related disorder				24291113;16301704;30027834;30279520;17224476;28427417;28490369;29759541;29697308		False	3	50;25;25	3.16	False		ENSG00000151067	ENSG00000151067	HGNC:1390													
KCNH2	gene	KCNH2	Brugada syndrome (Version 1.7);Emory Genetics Laboratory;Expert Review Green;Literature;London South GLH;Long QT syndrome (Version 1.5);North West GLH;Radboud University Medical Center, Nijmegen;South West GLH;UKGTN;West Midlands, Oxford and Wessex GLH	Short QT syndrome		Cardiology	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Brugada;Short QT syndrome 1 (609620);ventricular fibrillation;cardiac arrest;Short QT syndrome 1 609620;Long QT syndrome-2 (613688);short qt;atrial fibrillation				16226079;16301704;4676148;15828882;19340359;18692916;21130771;25974115;29016797;29759541;16011830;19439805;22194679;16039272;29085299		False	3	71;14;14	3.16	False	Other	ENSG00000055118	ENSG00000055118	HGNC:6251													
KCNJ2	gene	KCNJ2	Emory Genetics Laboratory;Expert Review Green;Literature;London South GLH;Long QT syndrome (Version 1.5);North West GLH;Radboud University Medical Center, Nijmegen;South West GLH;UKGTN;West Midlands, Oxford and Wessex GLH	Short QT syndrome		Cardiology	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Short QT syndrome 3, OMIM:609622;Short QT syndrome type 3, MONDO:0012314;Atrial fibrillation, familial, 9, OMIM:613980;Atrial fibrillation, familial, 9, MONDO:0013513;Andersen syndrome, OMIM:170390;Andersen-Tawil syndrome, MONDO:0008222				16226079;16301704;15761194;22155372;23440193;24794859;22311718;22308236;19285083;19710529;25691870		False	3	57;14;29	3.16	False	Other	ENSG00000123700	ENSG00000123700	HGNC:6263													
KCNQ1	gene	KCNQ1	Emory Genetics Laboratory;Expert Review Green;London South GLH;Long QT syndrome (Version 1.5);North West GLH;Other;Radboud University Medical Center, Nijmegen;South West GLH;UKGTN;West Midlands, Oxford and Wessex GLH	Short QT syndrome		Cardiology	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Short QT syndrome 2, OMIM:609621;Long QT syndrome-1, OMIM:192500;Atrial fibrillation, familial, 3, OMIM:607554				16226079;16301704;15159330;16109388;26168993;26346102;25974115;29697308		False	3	62;38;0	3.16	True		ENSG00000053918	ENSG00000053918	HGNC:6294