ClinVar Miner

Submissions for variant NM_000891.3(KCNJ2):c.*2752T>C

gnomAD frequency: 0.04719  dbSNP: rs993085233
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
GeneDx RCV001658399 SCV001871783 benign not provided 2021-05-13 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002495981 SCV002802703 benign Andersen Tawil syndrome; Short QT syndrome type 3; Atrial fibrillation, familial, 9 2021-08-17 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001658399 SCV005249406 benign not provided criteria provided, single submitter not provided

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.