ClinVar Miner

List of variants in gene combination LOC129390903, RAD51C reported as uncertain significance for Breast and/or ovarian cancer

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Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_058216.3(RAD51C):c.640C>T (p.Arg214Cys)	rs140804406	0.00017
NM_058216.3(RAD51C):c.620A>G (p.His207Arg)	rs587781921	0.00001

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