ClinVar Miner

Submissions for variant NM_002878.4(RAD51D):c.939C>A (p.Thr313=)

dbSNP: rs374318553
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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 RCV000776661 SCV000912284 likely benign Hereditary cancer-predisposing syndrome 2017-10-16 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002067339 SCV002439115 likely benign Breast-ovarian cancer, familial, susceptibility to, 4 2024-12-18 criteria provided, single submitter clinical testing

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