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

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Total variants: 17

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HGVS	dbSNP	gnomAD frequency
NM_058216.3(RAD51C):c.572-17G>T	rs193023469	0.00513
NM_058216.3(RAD51C):c.790G>A (p.Gly264Ser)	rs147241704	0.00207
NM_058216.3(RAD51C):c.1062A>G (p.Ala354=)	rs201000407	0.00004
NM_058216.3(RAD51C):c.546T>G (p.Leu182=)	rs1476282276	0.00004
NM_058216.3(RAD51C):c.705+14T>C	rs771168730	0.00003
NM_058216.3(RAD51C):c.706-13C>G	rs747406535	0.00003
NM_058216.3(RAD51C):c.905-19T>C	rs368114768	0.00003
NM_058216.3(RAD51C):c.1089G>A (p.Leu363=)	rs559647198	0.00002
NM_058216.3(RAD51C):c.234A>G (p.Thr78=)	rs730881929	0.00001
NM_058216.3(RAD51C):c.537C>T (p.His179=)	rs372385738	0.00001
NM_058216.3(RAD51C):c.79C>T (p.Leu27=)	rs786201775	0.00001
NM_058216.3(RAD51C):c.904+16G>C	rs929872458	0.00001
NM_058216.3(RAD51C):c.905-7C>T	rs757624360	0.00001
NM_058216.3(RAD51C):c.146-15T>C	rs1036386535
NM_058216.3(RAD51C):c.404+16C>T	rs376465837
NM_058216.3(RAD51C):c.838-20C>G	rs766600284
NM_058216.3(RAD51C):c.905-20A>G	rs950351911

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