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
HCN4	gene	HCN4	Expert Review Green;Victorian Clinical Genetics Services	Sick sinus syndrome		Cardiovascular disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sick sinus syndrome 2, MIM# 163800			Sick sinus syndrome;HP:0011704	12750403;15123648;16407510;17646576;25145518		False	3	100;0;0	1.4	True		ENSG00000138622	ENSG00000138622	HGNC:16882													
POPDC2	gene	POPDC2	Expert Review Green;Other	Sick sinus syndrome		Cardiovascular disorders	BIALLELIC, autosomal or pseudoautosomal	Sinoatrial node disorder, MONDO:0000469, POPDC2-related			Sick sinus syndrome;HP:0011704			False	3	100;0;0	1.4	True		ENSG00000121577	ENSG00000121577	HGNC:17648													
SCN5A	gene	SCN5A	Expert Review Green;Victorian Clinical Genetics Services	Sick sinus syndrome		Cardiovascular disorders	BIALLELIC, autosomal or pseudoautosomal	Sick sinus syndrome 1, MIM# 608567			Sick sinus syndrome;HP:0011704	14523039		False	3	100;0;0	1.4	True		ENSG00000183873	ENSG00000183873	HGNC:10593