ClinVar Miner

Submissions for variant NM_001375567.1(FOCAD):c.1176T>C (p.Cys392=)

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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 RCV005106131 SCV005730277 likely benign not provided 2024-11-12 criteria provided, single submitter clinical testing

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