ClinVar Miner

Submissions for variant NM_000166.6(GJB1):c.837C>G (p.Arg279=)

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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 RCV003583142 SCV004331621 likely benign Charcot-Marie-Tooth Neuropathy X 2023-10-12 criteria provided, single submitter clinical testing

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