ClinVar Miner

Submissions for variant NM_000891.2(KCNJ2):c.*3618A>G (rs530574251)

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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 RCV000323696 SCV000406204 likely benign short QT syndrome 2016-06-14 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000362020 SCV000406205 likely benign Andersen Tawil syndrome 2016-06-14 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000264986 SCV000406206 likely benign Familial atrial fibrillation 2016-06-14 criteria provided, single submitter clinical testing

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