ClinVar Miner

Submissions for variant NM_058216.3(RAD51C):c.146-9del

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV003018814 SCV003312014 benign Fanconi anemia complementation group O 2022-02-14 criteria provided, single submitter clinical testing

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