ClinVar Miner

Submissions for variant NM_000890.5(KCNJ5):c.*378dup

dbSNP: rs397799938
Minimum review status: Collection method:
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ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000407864 SCV000368967 benign Familial hyperaldosteronism 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000311867 SCV000368968 benign Congenital long QT syndrome 2016-06-14 criteria provided, single submitter clinical testing

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