ClinVar Miner

Submissions for variant NM_000890.5(KCNJ5):c.-293GA[3]

dbSNP: rs886047996
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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 RCV000268155 SCV000368867 uncertain significance Congenital long QT syndrome 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000302247 SCV000368868 uncertain significance Familial hyperaldosteronism 2016-06-14 criteria provided, single submitter clinical testing
GeneDx RCV001805010 SCV002050464 likely benign not provided 2021-05-22 criteria provided, single submitter clinical testing

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