ClinVar Miner

Submissions for variant NM_058216.3(RAD51C):c.838-18T>A

dbSNP: rs1567808119
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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 RCV000776655 SCV000912277 likely benign Hereditary cancer-predisposing syndrome 2017-10-13 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002067338 SCV002419884 likely benign Fanconi anemia complementation group O 2022-12-05 criteria provided, single submitter clinical testing

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