ClinVar Miner

List of variants reported as pathogenic for intracranial arterial disease by Victorian Clinical Genetics Services, Murdoch Childrens Research Institute

Included ClinVar conditions (12):

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_001256071.3(RNF213):c.14429G>A (p.Arg4810Lys)	rs112735431	0.00004
NM_001256071.3(RNF213):c.12353C>T (p.Ser4118Phe)	rs2079443410

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