ClinVar Miner

List of variants reported as pathogenic for Fanconi anemia complementation group O by Department of Pathology and Laboratory Medicine, Sinai Health System

Included ClinVar conditions (2):

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_058216.3(RAD51C):c.905-2_905-1del	rs587781995	0.00001
NM_058216.3(RAD51C):c.914G>A (p.Trp305Ter)	rs876659874	0.00001
NM_058216.3(RAD51C):c.158_160delinsTT (p.Ser53fs)	rs2047940629

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