ClinVar Miner

Submissions for variant NM_001040151.2(SCN3B):c.192C>T (p.Tyr64=)

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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 RCV003499841 SCV004354490 likely benign Brugada syndrome 7 2023-09-29 criteria provided, single submitter clinical testing

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