ClinVar Miner

Submissions for variant NM_000335.5(SCN5A):c.5798G>A (p.Ser1933Asn)

dbSNP: rs730880209
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Fulgent Genetics, Fulgent Genetics RCV002478472 SCV002789031 uncertain significance 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 2022-04-20 criteria provided, single submitter clinical testing
Blueprint Genetics RCV000157492 SCV000207237 uncertain significance Primary familial hypertrophic cardiomyopathy 2014-10-07 no assertion criteria provided clinical testing

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