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
FLNA	gene	FLNA	Expert Review Amber;Literature	Spontaneous coronary artery dissection		Cardiovascular disorders	X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)	Spontaneous coronary artery dissection				29334594		False	2	0;100;0	0.56	True		ENSG00000196924	ENSG00000196924	HGNC:3754													
LOX	gene	LOX	Expert Review Amber;Literature	Spontaneous coronary artery dissection		Cardiovascular disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	"Aortic aneurysm, familial thoracic 10	MIM#617168"				32897753;36103205		False	2	0;100;0	0.56	True		ENSG00000113083	ENSG00000113083	HGNC:6664													
MYLK	gene	MYLK	Expert Review Amber;Literature	Spontaneous coronary artery dissection		Cardiovascular disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	"Aortic aneurysm, familial thoracic 7	MIM#613780"				33125268		False	2	0;100;0	0.56	True		ENSG00000065534	ENSG00000065534	HGNC:7590													
TGFBR1	gene	TGFBR1	Expert Review Amber;Radboud University Medical Center, Nijmegen	Spontaneous coronary artery dissection		Cardiovascular disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	"Loeys-Dietz syndrome 1	MIM#609192"				35092149;36103205		False	2	0;100;0	0.56	True		ENSG00000106799	ENSG00000106799	HGNC:11772													
TLN1	gene	TLN1	Expert Review Amber;Literature	Spontaneous coronary artery dissection		Cardiovascular disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	idiopathic spontaneous coronary artery dissection MONDO:0007385				30888838;36103205		False	2	0;100;0	0.56	True		ENSG00000137076	ENSG00000137076	HGNC:11845													
YY1AP1	gene	YY1AP1	Expert Review Amber;Literature	Spontaneous coronary artery dissection		Cardiovascular disorders	BIALLELIC, autosomal or pseudoautosomal	Grange syndrome, MIM# 602531				33125268		False	2	0;100;0	0.56	True		ENSG00000163374	ENSG00000163374	HGNC:30935