ClinVar Miner

Submissions for variant NM_000890.5(KCNJ5):c.-289GA[18]

dbSNP: rs71057905
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000398967 SCV000368901 uncertain significance Congenital long QT syndrome 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000278502 SCV000368902 uncertain significance Familial hyperaldosteronism 2016-06-14 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002480106 SCV002781768 uncertain significance Long QT syndrome 13; Familial hyperaldosteronism type III 2021-07-13 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004693021 SCV005191574 uncertain significance not provided criteria provided, single submitter not provided

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