ClinVar Miner

Submissions for variant NM_000890.5(KCNJ5):c.*861GTTTT[8]

dbSNP: rs36205004
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 3
Download table as spreadsheet
Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000399885 SCV000368987 uncertain significance Familial hyperaldosteronism 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000309192 SCV000368988 uncertain significance Congenital long QT syndrome 2016-06-14 criteria provided, single submitter clinical testing
GeneDx RCV001597053 SCV001830721 benign not provided 2021-05-14 criteria provided, single submitter clinical testing

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.