ClinVar Miner

Submissions for variant NM_002878.4(RAD51D):c.668-8T>C

dbSNP: rs2142418939
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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 RCV002159730 SCV002340353 likely benign Breast-ovarian cancer, familial, susceptibility to, 4 2021-03-02 criteria provided, single submitter clinical testing
Sema4, Sema4 RCV002256899 SCV002534843 uncertain significance Hereditary cancer-predisposing syndrome 2021-09-09 criteria provided, single submitter curation

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