ClinVar Miner

Submissions for variant NM_000335.5(SCN5A):c.4264G>A (p.Asp1422Asn)

dbSNP: rs746291609
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Total submissions: 8
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Blueprint Genetics RCV000208284 SCV000264210 uncertain significance Primary dilated cardiomyopathy 2015-01-08 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000276067 SCV000443956 uncertain significance Sick sinus syndrome 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000333482 SCV000443957 uncertain significance Paroxysmal familial ventricular fibrillation 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000385583 SCV000443958 uncertain significance Dilated Cardiomyopathy, Dominant 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000274848 SCV000443959 uncertain significance Long QT syndrome 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000318130 SCV000443960 uncertain significance Congenital long QT syndrome 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000375017 SCV000443961 uncertain significance Brugada syndrome 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000278247 SCV000443962 uncertain significance Progressive familial heart block 2016-06-14 criteria provided, single submitter clinical testing

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