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
LMX1B	gene	LMX1B	Expert Review Red;Literature	Spontaneous coronary artery dissection		Cardiovascular disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	"Nail-patella syndrome	MIM#161200"				29650765		False	1	0;50;50	0.56	True		ENSG00000136944	ENSG00000136944	HGNC:6654													
PKD1	gene	PKD1	Expert Review Red;Literature	Spontaneous coronary artery dissection		Cardiovascular disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	"Polycystic kidney disease 1	MIM#173900"				35630097;26798684;26971055;29650765		False	1	50;0;50	0.56	True		ENSG00000008710	ENSG00000008710	HGNC:9008													
PTGIR	gene	PTGIR	Expert Review Red;Literature	Spontaneous coronary artery dissection		Cardiovascular disorders	Unknown					32531060		False	1	0;0;100	0.56	True		ENSG00000160013	ENSG00000160013	HGNC:9602													
TSR1	gene	TSR1	Expert Review Red;Literature	Spontaneous coronary artery dissection		Cardiovascular disorders	Unknown					PMID: 31296288;31296287;37979122		False	1	0;0;100	0.56	True		ENSG00000167721	ENSG00000167721	HGNC:25542													
