ClinVar Miner

Submissions for variant NM_058216.3(RAD51C):c.894T>G (p.Val298=)

dbSNP: rs1555602147
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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 RCV000582792 SCV000691281 likely benign Hereditary cancer-predisposing syndrome 2017-10-12 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV003507298 SCV004329280 likely benign Fanconi anemia complementation group O 2023-10-22 criteria provided, single submitter clinical testing

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