ClinVar Miner

Submissions for variant NM_002878.4(RAD51D):c.481-11C>T

gnomAD frequency: 0.00001  dbSNP: rs372690151
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001720016 SCV000516104 likely benign not provided 2019-07-10 criteria provided, single submitter clinical testing
Color Diagnostics, LLC DBA Color Health RCV000580160 SCV000686459 likely benign Hereditary cancer-predisposing syndrome 2016-05-17 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002061614 SCV002415628 likely benign Breast-ovarian cancer, familial, susceptibility to, 4 2025-01-30 criteria provided, single submitter clinical testing
Sema4, Sema4 RCV000580160 SCV002534819 likely benign Hereditary cancer-predisposing syndrome 2022-02-20 criteria provided, single submitter curation

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