ClinVar Miner

Submissions for variant NM_000890.5(KCNJ5):c.-295GA[3]

dbSNP: rs886047994
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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 RCV000335459 SCV000368857 uncertain significance Congenital long QT syndrome 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000400789 SCV000368858 uncertain significance Familial hyperaldosteronism 2016-06-14 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004693020 SCV005191572 uncertain significance not provided criteria provided, single submitter not provided

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