ClinVar Miner

Submissions for variant NM_000890.5(KCNJ5):c.*1323del

dbSNP: rs886048020
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000377179 SCV000369021 uncertain significance Congenital long QT syndrome 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000285077 SCV000369022 uncertain significance Familial hyperaldosteronism 2016-06-14 criteria provided, single submitter clinical testing

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