List of variants in gene RAD51C reported as likely benign for Breast and/or ovarian cancer

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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: 8

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HGVS	dbSNP	gnomAD frequency
NM_058216.3(RAD51C):c.790G>A (p.Gly264Ser)	rs147241704	0.00182
NM_058216.3(RAD51C):c.837+13T>C	rs188613030	0.00103
NM_058216.3(RAD51C):c.571+16A>G	rs141621051	0.00030
NM_058216.3(RAD51C):c.336G>A (p.Gly112=)	rs746122031	0.00005
NM_058216.3(RAD51C):c.870T>A (p.Ile290=)	rs376402418	0.00005
NM_058216.3(RAD51C):c.706-13C>G	rs747406535	0.00003
NM_058216.3(RAD51C):c.513C>T (p.Asp171=)	rs140279158	0.00002
NM_058216.3(RAD51C):c.945T>C (p.Phe315=)	rs201235884	0.00002

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