ClinVar Miner

Submissions for variant NM_002878.4(RAD51D):c.83-20T>C

gnomAD frequency: 0.00002  dbSNP: rs182793287
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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 RCV000582987 SCV000691370 likely benign Hereditary cancer-predisposing syndrome 2016-08-05 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002061936 SCV002405695 benign Breast-ovarian cancer, familial, susceptibility to, 4 2025-01-15 criteria provided, single submitter clinical testing

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