ClinVar Miner

Submissions for variant NM_004588.5(SCN2B):c.354G>A (p.Gln118=)

gnomAD frequency: 0.00001  dbSNP: rs752863331
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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 RCV001455208 SCV001658966 likely benign Atrial fibrillation, familial, 14 2021-02-02 criteria provided, single submitter clinical testing

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