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
ANO1	gene	ANO1	Expert Review Amber;Literature	Stroke		Neurology and neurodevelopmental disorders	MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	Moyamoya disease 7, MIM# 620687			Stroke;HP:0001297	PMID: 37253099		False	2	0;100;0	1.16	True		ENSG00000131620	ENSG00000131620	HGNC:21625													
CST3	gene	CST3	Expert Review Amber;Royal Melbourne Hospital	Stroke		Neurology and neurodevelopmental disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Cerebral amyloid angiopathy, MIM# 105150			Stroke;HP:0001297	3495457		False	2	0;100;0	1.16	True		ENSG00000101439	ENSG00000101439	HGNC:2475													
FLNA	gene	FLNA	Expert Review Amber;Royal Melbourne Hospital	Stroke		Neurology and neurodevelopmental disorders	Other	Heterotopia, periventricular, 1 , MIM#300049;Melnick-Needles syndrome 30, MIM#9350			Stroke;HP:0001297	21031081		False	2	0;100;0	1.16	True		ENSG00000196924	ENSG00000196924	HGNC:3754