ClinVar Miner

Submissions for variant NM_002878.4(RAD51D):c.741G>C (p.Val247=)

dbSNP: rs757986080
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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 RCV001179167 SCV001343778 likely benign Hereditary cancer-predisposing syndrome 2018-12-20 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001497818 SCV001702555 likely benign Breast-ovarian cancer, familial, susceptibility to, 4 2024-03-05 criteria provided, single submitter clinical testing

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