ClinVar Miner

Submissions for variant NM_000890.5(KCNJ5):c.-293_-289delinsGAGAGAGAGAGAA

dbSNP: rs886047999
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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 RCV000299424 SCV000368885 uncertain significance Congenital long QT syndrome 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000356627 SCV000368886 uncertain significance Familial hyperaldosteronism 2016-06-14 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002504061 SCV002815998 uncertain significance Long QT syndrome 13; Familial hyperaldosteronism type III 2021-08-19 criteria provided, single submitter clinical testing

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