List of variants reported as uncertain significance for breast-ovarian cancer, familial, susceptibility to, 4 by Fulgent Genetics, Fulgent Genetics

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Total variants: 10

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HGVS	dbSNP	gnomAD frequency
NM_002878.4(RAD51D):c.434G>A (p.Arg145His)	rs147264215	0.00023
NM_002878.4(RAD51D):c.263+1641C>T	rs142387263	0.00006
NM_002878.4(RAD51D):c.715C>T (p.Arg239Trp)	rs770250516	0.00006
NM_002878.4(RAD51D):c.793G>A (p.Gly265Arg)	rs140285068	0.00004
NM_002878.4(RAD51D):c.620C>T (p.Ser207Leu)	rs370228071	0.00002
NM_002878.4(RAD51D):c.80C>A (p.Thr27Lys)	rs139642328	0.00001
NM_001142571.2(RAD51D):c.-279_-275del	rs761104531
NM_002878.4(RAD51D):c.265C>T (p.Leu89Phe)	rs2142437449
NM_002878.4(RAD51D):c.680T>C (p.Met227Thr)	rs773485482
NM_002878.4(RAD51D):c.874A>G (p.Met292Val)	rs1555567076

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