ClinVar Miner

Submissions for variant NM_002878.4(RAD51D):c.709C>T (p.Leu237=)

dbSNP: rs1555567510
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001412424 SCV001614507 likely benign Breast-ovarian cancer, familial, susceptibility to, 4 2024-08-19 criteria provided, single submitter clinical testing
Hereditary Cancer Group, L’Institut d'Investigació Biomèdica de Bellvitge RCV001779166 SCV001623553 likely benign Breast-ovarian cancer, familial, susceptibility to, 3 2021-05-10 criteria provided, single submitter curation

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