ClinVar Miner

Submissions for variant NM_058216.3(RAD51C):c.978G>A (p.Leu326=)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Center for Genomic Medicine, Rigshospitalet, Copenhagen University Hospital RCV003494206 SCV004242888 likely benign not specified 2025-03-04 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV005062994 SCV005707537 likely benign Fanconi anemia complementation group O 2024-08-13 criteria provided, single submitter clinical testing

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