ClinVar Miner

Submissions for variant NM_001037.5(SCN1B):c.78G>A (p.Ser26=)

dbSNP: rs774401364
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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 RCV001460380 SCV001664248 likely benign Brugada syndrome 5 2022-12-09 criteria provided, single submitter clinical testing

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