List of variants in gene combination LOC129390903, RAD51C reported as likely benign for breast-ovarian cancer, familial, susceptibility to, 3

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 4

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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.635G>A (p.Arg212His)	rs200857129	0.00004
NM_058216.3(RAD51C):c.705+14T>C	rs771168730	0.00003
NM_058216.3(RAD51C):c.621T>A (p.His207Gln)	rs786201848	0.00001

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