ClinVar Miner

Submissions for variant NM_000283.4(PDE6B):c.2550C>T (p.Thr850=)

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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 RCV003724779 SCV004514639 likely benign not provided 2022-11-26 criteria provided, single submitter clinical testing

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