ClinVar Miner

Submissions for variant NM_002878.4(RAD51D):c.141C>T (p.Tyr47=)

dbSNP: rs771077929
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Color Diagnostics, LLC DBA Color Health RCV001181230 SCV001346330 likely benign Hereditary cancer-predisposing syndrome 2019-08-21 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV003769983 SCV004619420 likely benign Breast-ovarian cancer, familial, susceptibility to, 4 2023-04-26 criteria provided, single submitter clinical testing

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