ClinVar Miner

Submissions for variant NM_000891.2(KCNJ2):c.*558C>T (rs9302914)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Clinical Services Laboratory,Illumina RCV000339443 SCV000406030 benign Familial atrial fibrillation 2016-06-14 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000392706 SCV000406031 benign Andersen Tawil syndrome 2016-06-14 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000305629 SCV000406032 benign short QT syndrome 2016-06-14 criteria provided, single submitter clinical testing

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