ClinVar Miner

Submissions for variant NM_000890.5(KCNJ5):c.-293_-288del

dbSNP: rs886047997
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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 RCV000261502 SCV000368873 uncertain significance Congenital long QT syndrome 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000333106 SCV000368874 uncertain significance Familial hyperaldosteronism 2016-06-14 criteria provided, single submitter clinical testing
GeneDx RCV001636865 SCV001851614 benign not provided 2021-05-14 criteria provided, single submitter clinical testing

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