ClinVar Miner

Submissions for variant NM_058216.3(RAD51C):c.905-13T>G

dbSNP: rs2049019457
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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 RCV001176387 SCV001340360 uncertain significance Hereditary cancer-predisposing syndrome 2018-12-04 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV003769878 SCV004625090 likely benign Fanconi anemia complementation group O 2023-09-27 criteria provided, single submitter clinical testing

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