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
CLCA2	gene	CLCA2	Expert Review Amber;NHS GMS	Progressive cardiac conduction disease		Cardiology	MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	Heart conduction disease, MONDO:0000992						False	2	0;100;0	2.13	False		ENSG00000137975	ENSG00000137975	HGNC:2016													
SCN1B	gene	SCN1B	Expert Review Amber;London South GLH;South West GLH	Progressive cardiac conduction disease		Cardiology	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Cardiac conduction defect, nonspecific, OMIM:612838;Brugada syndrome 5, OMIM:612838;Atrial fibrillation, familial, 13, OMIM:615377				18464934;28878239;25426816		False	2	0;100;0	2.13	False		ENSG00000105711	ENSG00000105711	HGNC:10586													
TBX5	gene	TBX5	Expert Review Amber;London South GLH;South West GLH	Progressive cardiac conduction disease		Cardiology	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Holt-Oram syndrome, OMIM:142900				29755943		False	2	40;60;0	2.13	False		ENSG00000089225	ENSG00000089225	HGNC:11604													
TRPM4	gene	TRPM4	Expert Review Amber;London South GLH;South West GLH;Wessex and West Midlands GLH	Progressive cardiac conduction disease		Cardiology	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Progressive familial heart block, type IB, OMIM:604559				19726882;20562447;21887725;29748318;30021168;29568272		False	2	50;50;0	2.13	False		ENSG00000130529	ENSG00000130529	HGNC:17993