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
C4A	gene	C4A	Expert Review Amber;Victorian Clinical Genetics Services	Vasculitis		Immunological disorders	Other	C4a deficiency MIM#614380;susceptibility systemic lupus erythematosus				22387014;22737222;15998580;10529130;15294999;32048120		False	2	0;100;0	0.86	True		ENSG00000244731	ENSG00000244731	HGNC:1323													
C8A	gene	C8A	Expert Review Amber;Victorian Clinical Genetics Services	Vasculitis		Immunological disorders	BIALLELIC, autosomal or pseudoautosomal	C8 deficiency, type I MIM#613790				9759902;32769119		False	2	0;100;0	0.86	True		ENSG00000157131	ENSG00000157131	HGNC:1352													
CST3	gene	CST3	Expert Review Amber;Victorian Clinical Genetics Services	Vasculitis		Immunological disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Cerebral amyloid angiopathy, MIM# 105150				3495457		False	2	0;100;0	0.86	True		ENSG00000101439	ENSG00000101439	HGNC:2475													
HCK	gene	HCK	Expert Review;Expert Review Amber	Vasculitis		Immunological disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Autoinflammation with pulmonary and cutaneous vasculitis, MIM#620296				34536415		False	2	0;100;0	0.86	True	Other	ENSG00000101336	ENSG00000101336	HGNC:4840