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
CORIN	gene	CORIN	Expert list;Expert Review Red	Atrial Fibrillation		Cardiovascular disorders	BIALLELIC, autosomal or pseudoautosomal	?Cardiomyopathy, familial hypertrophic, 30, atrial (MIM:620734)			Atrial fibrillation;HP:0005110	37913506;15637153		False	1	0;0;100	1.2	True		ENSG00000145244	ENSG00000145244	HGNC:19012													
KCNE5	gene	KCNE5	Expert Review Red;Victorian Clinical Genetics Services	Atrial Fibrillation		Cardiovascular disorders	X-LINKED: hemizygous mutation in males, biallelic mutations in females	Atrial fibrillation			Atrial fibrillation;HP:0005110	18313602;16054468;30289750		False	1	0;0;100	1.2	True		ENSG00000176076	ENSG00000176076	HGNC:6241													
SHOX2	gene	SHOX2	Expert Review;Expert Review Red	Atrial Fibrillation		Cardiovascular disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sinus Node Dysfunction;Atrial Fibrillation			Atrial fibrillation;HP:0005110	30443179		False	1	0;0;100	1.2	True		ENSG00000168779	ENSG00000168779	HGNC:10854