ClinVar Miner

Submissions for variant NM_002878.4(RAD51D):c.834G>C (p.Leu278=)

dbSNP: rs876658123
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000936457 SCV001082225 likely benign Breast-ovarian cancer, familial, susceptibility to, 4 2024-08-19 criteria provided, single submitter clinical testing
Color Diagnostics, LLC DBA Color Health RCV003584781 SCV004357147 likely benign Hereditary cancer-predisposing syndrome 2022-02-16 criteria provided, single submitter clinical testing

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