ClinVar Miner

Submissions for variant NM_002878.4(RAD51D):c.577-13C>A

gnomAD frequency: 0.00001  dbSNP: rs748697766
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Color Diagnostics, LLC DBA Color Health RCV000582994 SCV000691347 likely benign Hereditary cancer-predisposing syndrome 2015-08-26 criteria provided, single submitter clinical testing
GeneDx RCV001722540 SCV000732180 likely benign not provided 2020-04-28 criteria provided, single submitter clinical testing This variant is associated with the following publications: (PMID: 25980754)
Labcorp Genetics (formerly Invitae), Labcorp RCV002061931 SCV002446709 likely benign Breast-ovarian cancer, familial, susceptibility to, 4 2024-10-02 criteria provided, single submitter clinical testing

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