List of variants in gene combination RAD51D, RAD51L3-RFFL reported as uncertain significance 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: 13

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HGVS	dbSNP	gnomAD frequency
NM_002878.4(RAD51D):c.26G>C (p.Cys9Ser)	rs140825795	0.00037
NM_002878.4(RAD51D):c.167T>G (p.Val56Gly)	rs745307359	0.00033
NM_002878.4(RAD51D):c.413A>G (p.Asn138Ser)	rs201676898	0.00025
NM_002878.4(RAD51D):c.137C>G (p.Ser46Cys)	rs587780102	0.00010
NM_002878.4(RAD51D):c.355T>C (p.Cys119Arg)	rs201313861	0.00008
NM_002878.4(RAD51D):c.145-4G>A	rs201361465	0.00006
NM_002878.4(RAD51D):c.346-10C>T	rs779972784	0.00005
NM_002878.4(RAD51D):c.185C>T (p.Ser62Leu)	rs374357106	0.00004
NM_002878.4(RAD51D):c.493C>T (p.Arg165Trp)	rs544654228	0.00004
NM_002878.4(RAD51D):c.793G>A (p.Gly265Arg)	rs140285068	0.00004
NM_002878.4(RAD51D):c.796C>T (p.Arg266Cys)	rs587781813	0.00004
NM_002878.4(RAD51D):c.667+9T>C	rs772193051	0.00001
NM_002878.4(RAD51D):c.766G>C (p.Asp256His)	rs1567725026

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