List of variants reported as likely pathogenic for Breast-ovarian cancer, familial, susceptibility to, 3; Fanconi anemia complementation group O by Fulgent Genetics, Fulgent Genetics

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Total variants: 12

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HGVS	dbSNP	gnomAD frequency
NM_058216.3(RAD51C):c.404+2T>C	rs730881931	0.00001
NM_058216.3(RAD51C):c.414G>C (p.Leu138Phe)	rs267606999	0.00001
NM_058216.3(RAD51C):c.904+5G>T	rs587782702	0.00001
NM_058216.3(RAD51C):c.914G>A (p.Trp305Ter)	rs876659874	0.00001
NM_058216.3(RAD51C):c.146-2A>G	rs1555593457
NM_058216.3(RAD51C):c.250A>T (p.Lys84Ter)	rs1555593616
NM_058216.3(RAD51C):c.405-1G>C	rs587782036
NM_058216.3(RAD51C):c.472dup (p.Ile158fs)	rs2143746162
NM_058216.3(RAD51C):c.705+1G>A	rs876658644
NM_058216.3(RAD51C):c.706-2A>C	rs587780259
NM_058216.3(RAD51C):c.82dup (p.Val28fs)	rs2143677258
NM_058216.3(RAD51C):c.837+1G>T	rs760235677

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