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	Cardiac conduction disease		Cardiovascular disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	heart conduction disease MONDO:0000992			Cardiac conduction abnormality;HP:0031546	31326550		False	2	0;100;0	1.6	True		ENSG00000137975	ENSG00000137975	HGNC:2016													
GJA5	gene	GJA5	Expert Review Amber;NHS GMS	Cardiac conduction disease		Cardiovascular disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	heart conduction disease MONDO:0000992			Cardiac conduction abnormality;HP:0031546	9501069;10086977;22247482;36352534		False	2	0;100;0	1.6	True		ENSG00000143140	ENSG00000265107	HGNC:4279													
SCN1B	gene	SCN1B	Expert Review Amber;NHS GMS	Cardiac conduction disease		Cardiovascular disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Heart conduction disease MONDO:0000992			Cardiac conduction abnormality;HP:0031546	19808477;18464934;28878239;29758173		False	2	0;100;0	1.6	True		ENSG00000105711	ENSG00000105711	HGNC:10586													
TRPM4	gene	TRPM4	Expert Review Amber;NHS GMS	Cardiac conduction disease		Cardiovascular disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	progressive familial heart block type IB MONDO:0011474			Cardiac conduction abnormality;HP:0031546	41195386;19726882;26820365;21887725;32681584;20562447;25531103;27207958;29568272;29748318;36352534;35205305		False	2	0;100;0	1.6	True	Other	ENSG00000130529	ENSG00000130529	HGNC:17993