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
MYH11	gene	MYH11	Expert Review Red;Royal Melbourne Hospital	Stroke		Neurology and neurodevelopmental disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Aortic aneurysm, familial thoracic 4, MIM# 132900			Stroke;HP:0001297			False	1	0;0;100	1.16	True		ENSG00000133392	ENSG00000133392	HGNC:7569													
NOS3	gene	NOS3	Expert Review Red;Royal Melbourne Hospital	Stroke		Neurology and neurodevelopmental disorders	Unknown	{Ischemic stroke, susceptibility to} MIM#601367			Stroke;HP:0001297	24986538;28084234		False	1	0;0;100	1.16	True		ENSG00000164867	ENSG00000164867	HGNC:7876													
TRIM47	gene	TRIM47	Expert Review Red;Literature	Stroke		Neurology and neurodevelopmental disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Genetic cerebral small vessel disease MONDO:0018787			Stroke;HP:0001297	35511193		False	1	0;0;100	1.16	True		ENSG00000132481	ENSG00000132481	HGNC:19020													
WFS1	gene	WFS1	Expert Review Red;Royal Melbourne Hospital	Stroke		Neurology and neurodevelopmental disorders	BIALLELIC, autosomal or pseudoautosomal	Diabetes mellitus AND insipidus with optic atrophy AND deafness			Stroke;HP:0001297			False	1	0;0;100	1.16	True		ENSG00000109501	ENSG00000109501	HGNC:12762