ClinVar Miner

List of variants reported as likely benign by Hereditary Cancer Group, L’Institut d'Investigació Biomèdica de Bellvitge

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Total variants: 5
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HGVS dbSNP gnomAD frequency
NM_002878.4(RAD51D):c.167T>G (p.Val56Gly) rs745307359 0.00033
NM_002878.4(RAD51D):c.709C>T (p.Leu237=) rs1555567510
NM_058216.3(RAD51C):c.348C>G (p.Pro116=) rs2047955792
NM_058216.3(RAD51C):c.586T>C (p.Leu196=) rs2143796827
NM_058216.3(RAD51C):c.801G>A (p.Gln267=) rs2048499866

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