ClinVar Miner

Submissions for variant NM_198056.2(SCN5A):c.3384C>T (p.Cys1128=) (rs561922849)

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Total submissions: 10
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Clinical Services Laboratory,Illumina RCV000270423 SCV000443999 uncertain significance Long QT syndrome 2016-06-14 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000325445 SCV000444000 uncertain significance Romano-Ward syndrome 2016-06-14 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000384665 SCV000444001 uncertain significance Paroxysmal familial ventricular fibrillation 2016-06-14 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000290209 SCV000444002 uncertain significance Dilated Cardiomyopathy, Dominant 2016-06-14 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000331248 SCV000444003 uncertain significance Sick sinus syndrome 2016-06-14 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000385639 SCV000444004 uncertain significance Progressive familial heart block 2016-06-14 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000295960 SCV000444005 uncertain significance Brugada syndrome 2016-06-14 criteria provided, single submitter clinical testing
Color Health, Inc RCV001184785 SCV001350852 likely benign Arrhythmia 2018-11-25 criteria provided, single submitter clinical testing
Molecular Diagnostic Laboratory for Inherited Cardiovascular Disease,Montreal Heart Institute RCV001256855 SCV001433345 benign not specified 2020-03-20 criteria provided, single submitter clinical testing
Invitae RCV000295960 SCV001608315 likely benign Brugada syndrome 2020-09-24 criteria provided, single submitter clinical testing

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