ClinVar Miner

Submissions for variant NM_000283.4(PDE6B):c.2214T>C (p.Ala738=)

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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 RCV002711463 SCV003000589 likely benign not provided 2022-03-11 criteria provided, single submitter clinical testing

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