ClinVar Miner

Submissions for variant NM_006514.4(SCN10A):c.714C>T (p.Ala238=)

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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 RCV002700362 SCV002996376 likely benign Brugada syndrome 2024-02-24 criteria provided, single submitter clinical testing

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