ClinVar Miner

Submissions for variant NM_000891.3(KCNJ2):c.*1702_*1704dup

dbSNP: rs1555604193
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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 RCV000360714 SCV000406096 uncertain significance Familial atrial fibrillation 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000266077 SCV000406097 uncertain significance Short QT syndrome 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000302503 SCV000406098 uncertain significance Andersen Tawil syndrome 2016-06-14 criteria provided, single submitter clinical testing

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