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
CALM3	gene	CALM3	Expert Review Amber;Victorian Clinical Genetics Services	Arrhythmia_SuperPanel		Cardiovascular disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	"Ventricular tachycardia, catecholaminergic polymorphic 6, MIM#	618782"				27516456;31170290;31454269		False	2	33;33;33	5.1	True		ENSG00000160014	ENSG00000160014	HGNC:1449													
CAV3	gene	CAV3	Expert Review Amber;Victorian Clinical Genetics Services	Arrhythmia_SuperPanel		Cardiovascular disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Long QT syndrome 9, MIM# 611818				31983240;17060380		False	2	0;100;0	5.1	True		ENSG00000182533	ENSG00000182533	HGNC:1529													
CDH2	gene	CDH2	Expert Review Amber;Expert list	Arrhythmia_SuperPanel		Cardiovascular disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Arrhythmogenic right ventricular dysplasia, familial, 14, OMIM#618920						False	2	0;100;0	5.1	True		ENSG00000170558	ENSG00000170558	HGNC:1759													
CLCA2	gene	CLCA2	Expert Review Amber;NHS GMS	Arrhythmia_SuperPanel		Cardiovascular disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	heart conduction disease MONDO:0000992				31326550		False	2	0;100;0	5.1	True		ENSG00000137975	ENSG00000137975	HGNC:2016													
CTNNA3	gene	CTNNA3	Expert Review Amber;Other	Arrhythmia_SuperPanel		Cardiovascular disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	"Arrhythmogenic right ventricular cardiomyopathy;Arrhythmogenic right ventricular dysplasia, familial, 13	MIM#615616"				23136403;21254927;22421363;30415094;31539150		False	2	0;100;0	5.1	True		ENSG00000183230	ENSG00000183230	HGNC:2511													
GJA5	gene	GJA5	Expert Review Amber;NHS GMS	Arrhythmia_SuperPanel		Cardiovascular disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	heart conduction disease MONDO:0000992				9501069;10086977;22247482;36352534		False	2	0;100;0	5.1	True		ENSG00000143140	ENSG00000265107	HGNC:4279													
GJA5	gene	GJA5	Expert Review Amber;Victorian Clinical Genetics Services	Arrhythmia_SuperPanel		Cardiovascular disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Atrial fibrillation, familial, 11, OMIM# 614049				16790700;20818502;20650941;23348765		False	2	50;50;0	5.1	True		ENSG00000143140	ENSG00000265107	HGNC:4279													
KBTBD13	gene	KBTBD13	Expert Review Amber;Literature	Arrhythmia_SuperPanel		Cardiovascular disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Intrinsic cardiomyopathy MONDO:0000591				36335629		False	2	0;100;0	5.1	True		ENSG00000234438	ENSG00000234438	HGNC:37227													
KCNA5	gene	KCNA5	Expert Review Amber;Victorian Clinical Genetics Services	Arrhythmia_SuperPanel		Cardiovascular disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Atrial fibrillation, familial, 7, MIM# 612240				16772329;19343045;23264583		False	2	0;100;0	5.1	True		ENSG00000130037	ENSG00000130037	HGNC:6224													
KCNE1	gene	KCNE1	Expert Review Amber;Victorian Clinical Genetics Services	Arrhythmia_SuperPanel		Cardiovascular disorders	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	Jervell and Lange-Nielsen syndrome 2, MIM# 612347;Long QT syndrome 5, MIM# 613695;Acquired LQTS				31983240		False	2	0;100;0	5.1	True		ENSG00000180509	ENSG00000180509	HGNC:6240													
LEMD2	gene	LEMD2	Expert Review Amber;Literature	Arrhythmia_SuperPanel		Cardiovascular disorders	BIALLELIC, autosomal or pseudoautosomal	arrhythmogenic right ventricular cardiomyopathy, MONDO:0016587				31061923;26788539;30905398;36377660		False	2	0;100;0	5.1	True		ENSG00000161904	ENSG00000161904	HGNC:21244													
LMNA	gene	LMNA	Expert Review Amber;Expert list	Arrhythmia_SuperPanel		Cardiovascular disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	"Cardiomyopathy, dilated, 1A, MIM#	115200;Arrhythmogenic right ventricular cardiomyopathy"				22199124;25837155;26620845		False	2	0;100;0	5.1	True		ENSG00000160789	ENSG00000160789	HGNC:6636													
MYL4	gene	MYL4	Expert Review Amber;Literature	Arrhythmia_SuperPanel		Cardiovascular disorders	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	atrial fibrillation, familial, 18 MONDO:0015001				27742809;27066836;29080865		False	2	0;100;0	5.1	True		ENSG00000198336	ENSG00000198336	HGNC:7585													
NPPA	gene	NPPA	Expert Review Amber;Victorian Clinical Genetics Services	Arrhythmia_SuperPanel		Cardiovascular disorders	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	Atrial fibrillation, familial, 6, (MIM#612201)				18614783;20064500;31034774;31077706;23275345;40838933		False	2	0;100;0	5.1	True		ENSG00000175206	ENSG00000175206	HGNC:7939													
PLN	gene	PLN	Expert Review Amber;Expert list	Arrhythmia_SuperPanel		Cardiovascular disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Arrhythmogenic right ventricular cardiomyopathy				22820313;33831308		False	2	0;100;0	5.1	True		ENSG00000198523	ENSG00000198523	HGNC:9080													
SCN1B	gene	SCN1B	Expert Review Amber;NHS GMS	Arrhythmia_SuperPanel		Cardiovascular disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Heart conduction disease MONDO:0000992				19808477;18464934;28878239;29758173		False	2	0;100;0	5.1	True		ENSG00000105711	ENSG00000105711	HGNC:10586													
TAX1BP3	gene	TAX1BP3	Expert Review Amber;Literature	Arrhythmia_SuperPanel		Cardiovascular disorders	BIALLELIC, autosomal or pseudoautosomal	Familial cardiomyopathy, MONDO:0005217, TAX1BP3-related;arrhythmogenic cardiomyopathy				PMID: 39963794;25645515		False	2	0;100;0	5.1	True		ENSG00000213977	ENSG00000213977	HGNC:30684													
TRPM4	gene	TRPM4	Expert Review Amber;NHS GMS	Arrhythmia_SuperPanel		Cardiovascular disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	progressive familial heart block type IB MONDO:0011474				41195386;19726882;26820365;21887725;32681584;20562447;25531103;27207958;29568272;29748318;36352534;35205305		False	2	0;100;0	5.1	True	Other	ENSG00000130529	ENSG00000130529	HGNC:17993