ClinVar Miner

Submissions for variant NM_002878.4(RAD51D):c.675C>T (p.Ala225=)

dbSNP: rs760789270
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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 RCV000776987 SCV000912662 likely benign Hereditary cancer-predisposing syndrome 2017-12-05 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002067347 SCV002473475 likely benign Breast-ovarian cancer, familial, susceptibility to, 4 2022-01-17 criteria provided, single submitter clinical testing

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