ClinVar Miner

Submissions for variant NM_000891.3(KCNJ2):c.-88C>T

gnomAD frequency: 0.00004  dbSNP: rs886053322
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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 RCV000374282 SCV000405982 uncertain significance Short QT syndrome 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000284472 SCV000405983 uncertain significance Familial atrial fibrillation 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000339533 SCV000405984 uncertain significance Andersen Tawil syndrome 2016-06-14 criteria provided, single submitter clinical testing

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