ClinVar Miner

Submissions for variant NM_000891.3(KCNJ2):c.*3391_*3392dup

dbSNP: rs552636156
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000281253 SCV000406192 uncertain significance Andersen Tawil syndrome 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000338572 SCV000406193 uncertain significance Familial atrial fibrillation 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000402404 SCV000406194 uncertain significance Short QT syndrome 2016-06-14 criteria provided, single submitter clinical testing

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