ClinVar Miner

Submissions for variant NM_000891.3(KCNJ2):c.*2774_*2775del

dbSNP: rs35656864
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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 RCV000352322 SCV000406150 uncertain significance Short QT syndrome 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000388247 SCV000406151 uncertain significance Andersen Tawil syndrome 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000294371 SCV000406152 uncertain significance Familial atrial fibrillation 2016-06-14 criteria provided, single submitter clinical testing

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