ClinVar Miner

Submissions for variant NM_000335.5(SCN5A):c.168G>A (p.Leu56=)

dbSNP: rs376742447
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001445391 SCV001648422 likely benign Brugada syndrome 2018-10-03 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002502851 SCV002801884 likely benign Brugada syndrome 1; Long QT syndrome 3; Sick sinus syndrome 1; Progressive familial heart block, type 1A; Ventricular fibrillation, paroxysmal familial, type 1; Dilated cardiomyopathy 1E; SUDDEN INFANT DEATH SYNDROME; Atrial fibrillation, familial, 10 2021-07-26 criteria provided, single submitter clinical testing

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