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
GNB2	gene	GNB2	Expert list;Expert Review Red;Literature	Cardiac conduction disease		Cardiovascular disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sick sinus syndrome 4, MIM# 619464			Cardiac conduction abnormality;HP:0031546	28219978		False	1	0;0;100	1.6	False		ENSG00000172354	ENSG00000172354	HGNC:4398													
MRC2	gene	MRC2	Expert Review Red;Literature	Cardiac conduction disease		Cardiovascular disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Wolff-Parkinson-White syndrome - MONDO:0008685, MRC2-related			Cardiac conduction abnormality;HP:0031546	PMID - 38953222		False	1	0;0;100	1.6	True		ENSG00000011028	ENSG00000011028	HGNC:16875													
NNT	gene	NNT	Expert Review Red;Literature	Cardiac conduction disease		Cardiovascular disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	left ventricular noncompaction MONDO:0018901			Cardiac conduction abnormality;HP:0031546	26025024		False	1	0;0;100	1.6	True		ENSG00000112992	ENSG00000112992	HGNC:7863