ClinVar Miner

Submissions for variant NM_004588.5(SCN2B):c.567G>A (p.Gln189=)

dbSNP: rs2135517512
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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 RCV002169071 SCV002477415 likely benign Atrial fibrillation, familial, 14 2020-11-28 criteria provided, single submitter clinical testing

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