ClinVar Miner

Submissions for variant NM_058216.3(RAD51C):c.348C>T (p.Pro116=)

dbSNP: rs2047955792
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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 RCV001187427 SCV001354242 likely benign Hereditary cancer-predisposing syndrome 2018-11-05 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002068464 SCV002479842 likely benign Fanconi anemia complementation group O 2020-12-04 criteria provided, single submitter clinical testing

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