ClinVar Miner

Submissions for variant NM_058216.3(RAD51C):c.972A>G (p.Ala324=)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
CeGaT Center for Human Genetics Tuebingen RCV003334203 SCV004042011 uncertain significance not provided 2023-09-01 criteria provided, single submitter clinical testing RAD51C: PM2, BP4, BP7
Labcorp Genetics (formerly Invitae), Labcorp RCV003777415 SCV004612867 likely benign Fanconi anemia complementation group O 2024-07-09 criteria provided, single submitter clinical testing

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