ClinVar Miner

Submissions for variant NM_000891.2(KCNJ2):c.*2262C>T (rs575383136)

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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 RCV000272911 SCV000406123 likely benign Familial atrial fibrillation 2016-06-14 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000327997 SCV000406124 likely benign Andersen Tawil syndrome 2016-06-14 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000382521 SCV000406125 likely benign short QT syndrome 2016-06-14 criteria provided, single submitter clinical testing

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