ClinVar Miner

Submissions for variant NM_000785.4(CYP27B1):c.489C>T (p.Cys163=)

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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 RCV003664934 SCV004371978 likely benign not provided 2024-01-04 criteria provided, single submitter clinical testing

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