ClinVar Miner

Submissions for variant NM_000891.2(KCNJ2):c.*1069C>T (rs45603434)

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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 RCV000260363 SCV000406057 benign Familial atrial fibrillation 2016-06-14 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000317799 SCV000406058 benign short QT syndrome 2016-06-14 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000356255 SCV000406059 benign Andersen Tawil syndrome 2016-06-14 criteria provided, single submitter clinical testing

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