ClinVar Miner

Submissions for variant NM_004588.5(SCN2B):c.594C>T (p.Thr198=)

dbSNP: rs1326811641
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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 RCV001404706 SCV001606615 likely benign Atrial fibrillation, familial, 14 2020-08-25 criteria provided, single submitter clinical testing

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