ClinVar Miner

Submissions for variant NM_000890.5(KCNJ5):c.*1338C>A

gnomAD frequency: 0.27661  dbSNP: rs6590358
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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 RCV000279109 SCV000369025 benign Familial hyperaldosteronism 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000336476 SCV000369026 benign Congenital long QT syndrome 2016-06-14 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004706830 SCV005233475 benign not provided criteria provided, single submitter not provided

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