ClinVar Miner

Submissions for variant NM_000891.3(KCNJ2):c.*1678dup

dbSNP: rs145779709
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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 RCV000346150 SCV000406093 benign Andersen Tawil syndrome 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000392207 SCV000406094 benign Short QT syndrome 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000306463 SCV000406095 benign Familial atrial fibrillation 2016-06-14 criteria provided, single submitter clinical testing
GeneDx RCV001643013 SCV001860358 benign not provided 2021-06-03 criteria provided, single submitter clinical testing

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