ClinVar Miner

Submissions for variant NM_001037.5(SCN1B):c.448+8G>A

dbSNP: rs200222933
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001718868 SCV000514503 likely benign not provided 2019-03-15 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002061502 SCV002392537 likely benign Brugada syndrome 5 2024-09-25 criteria provided, single submitter clinical testing

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