ClinVar Miner

Submissions for variant NM_000890.5(KCNJ5):c.-289GA[19]

dbSNP: rs71057905
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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 RCV000337855 SCV000368903 uncertain significance Familial hyperaldosteronism 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000392268 SCV000368904 uncertain significance Congenital long QT syndrome 2016-06-14 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002480107 SCV002785640 uncertain significance Long QT syndrome 13; Familial hyperaldosteronism type III 2021-07-26 criteria provided, single submitter clinical testing

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