ClinVar Miner

Submissions for variant NM_000219.6(KCNE1):c.*1583A>C

dbSNP: rs886057018
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000269054 SCV000435695 uncertain significance Long QT syndrome 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000328021 SCV000435696 uncertain significance Congenital long QT syndrome 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000384908 SCV000435697 uncertain significance Jervell and Lange-Nielsen syndrome 2016-06-14 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002487500 SCV002792545 uncertain significance Jervell and Lange-Nielsen syndrome 2; Long QT syndrome 5 2021-09-20 criteria provided, single submitter clinical testing

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