ClinVar Miner

List of variants in gene combination ABCC8, KCNJ11 reported as uncertain significance for carbohydrate metabolism disease

Included ClinVar conditions (161):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 4
Download table as spreadsheet
HGVS dbSNP
NM_000525.3(KCNJ11):c.-154G>T rs539975714
NM_000525.3(KCNJ11):c.-498T>C rs529946415
NM_000525.3(KCNJ11):c.-559G>C rs547932593
NM_000525.3(KCNJ11):c.108G>A (p.Val36=) rs112070496

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.