ClinVar Miner

List of variants in gene combination RAD51D, RAD51L3-RFFL reported as likely benign by Women's Health and Genetics/Laboratory Corporation of America, LabCorp

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Total variants: 22
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HGVS dbSNP gnomAD frequency
NM_002878.4(RAD51D):c.146C>T (p.Ala49Val) rs140317560 0.00116
NM_002878.4(RAD51D):c.26G>C (p.Cys9Ser) rs140825795 0.00037
NM_002878.4(RAD51D):c.216C>T (p.Tyr72=) rs148690585 0.00028
NM_002878.4(RAD51D):c.413A>G (p.Asn138Ser) rs201676898 0.00025
NM_002878.4(RAD51D):c.39C>G (p.Thr13=) rs146448657 0.00018
NM_002878.4(RAD51D):c.864C>T (p.Gly288=) rs138557828 0.00009
NM_002878.4(RAD51D):c.145-4G>A rs201361465 0.00006
NM_002878.4(RAD51D):c.957G>A (p.Gln319=) rs147669627 0.00006
NM_002878.4(RAD51D):c.796C>T (p.Arg266Cys) rs587781813 0.00004
NM_002878.4(RAD51D):c.765G>A (p.Arg255=) rs751833940 0.00003
NM_002878.4(RAD51D):c.879G>A (p.Ala293=) rs368209468 0.00003
NM_002878.4(RAD51D):c.792C>G (p.Leu264=) rs536544621 0.00002
NM_002878.4(RAD51D):c.966A>G (p.Thr322=) rs786203299 0.00002
NM_002878.4(RAD51D):c.126A>G (p.Lys42=) rs145361433 0.00001
NM_002878.4(RAD51D):c.12C>G (p.Leu4=) rs786203193 0.00001
NM_002878.4(RAD51D):c.198G>T (p.Val66=) rs200810304 0.00001
NM_002878.4(RAD51D):c.22C>T (p.Leu8=) rs876659203 0.00001
NM_002878.4(RAD51D):c.382C>T (p.Leu128=) rs1438461174 0.00001
NM_002878.4(RAD51D):c.900A>G (p.Arg300=) rs370634278 0.00001
NM_002878.4(RAD51D):c.90C>T (p.Asp30=) rs374725981 0.00001
NM_002878.4(RAD51D):c.840C>T (p.Thr280=) rs751885496
NM_002878.4(RAD51D):c.879G>T (p.Ala293=) rs368209468

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