ClinVar Miner

Submissions for variant NM_001037.5(SCN1B):c.448+191A>G

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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 RCV002589976 SCV002956198 likely benign Brugada syndrome 5 2023-07-14 criteria provided, single submitter clinical testing

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