ClinVar Miner

Submissions for variant NM_004588.5(SCN2B):c.237+19G>A

gnomAD frequency: 0.00001  dbSNP: rs371565413
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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 RCV002147644 SCV002411317 likely benign Atrial fibrillation, familial, 14 2023-11-17 criteria provided, single submitter clinical testing

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