ClinVar Miner

Submissions for variant NM_000890.5(KCNJ5):c.*861GTTTT[7]

dbSNP: rs36205004
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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 RCV000366259 SCV000368989 benign Familial hyperaldosteronism 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000392654 SCV000368990 benign Congenital long QT syndrome 2016-06-14 criteria provided, single submitter clinical testing
GeneDx RCV001653488 SCV001867066 benign not provided 2021-05-12 criteria provided, single submitter clinical testing

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