ClinVar Miner

Submissions for variant NM_000283.4(PDE6B):c.540C>A (p.Ile180=)

dbSNP: rs2474104393
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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 RCV002811937 SCV003206822 likely benign not provided 2023-06-13 criteria provided, single submitter clinical testing

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