ClinVar Miner

Submissions for variant NM_000891.3(KCNJ2):c.579T>G (p.Leu193=)

gnomAD frequency: 0.00001  dbSNP: rs773272852
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
Download table as spreadsheet
Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001474074 SCV001678239 likely benign Andersen Tawil syndrome; Short QT syndrome type 3 2022-04-20 criteria provided, single submitter clinical testing
Women's Health and Genetics/Laboratory Corporation of America, LabCorp RCV003490256 SCV004242101 likely benign not specified 2023-12-10 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.