ClinVar Miner

Submissions for variant NM_000283.4(PDE6B):c.2391C>T (p.Phe797=)

dbSNP: rs143154045
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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 RCV001474848 SCV001679025 likely benign not provided 2024-09-23 criteria provided, single submitter clinical testing

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