ClinVar Miner

Submissions for variant NM_002878.4(RAD51D):c.904-13C>A

gnomAD frequency: 0.00001  dbSNP: rs964696175
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001693511 SCV001912739 benign not provided 2015-04-06 criteria provided, single submitter clinical testing
Color Diagnostics, LLC DBA Color Health RCV001806247 SCV002052892 likely benign Hereditary cancer-predisposing syndrome 2023-09-05 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002073239 SCV002476151 likely benign Breast-ovarian cancer, familial, susceptibility to, 4 2024-12-18 criteria provided, single submitter clinical testing
Sema4, Sema4 RCV001806247 SCV002527049 uncertain significance Hereditary cancer-predisposing syndrome 2021-12-09 criteria provided, single submitter curation

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