ClinVar Miner

Variants studied for Glomerulonephritis; Autoimmunity; Chronic gastritis; Gastritis; Crescentic glomerulonephritis; Chronic kidney disease; Thyroiditis; Type I diabetes mellitus; Autosomal dominant inheritance; Diabetes mellitus; X-linked dominant inheritance

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:

If a variant has more than one submission, it may be counted in more than one significance column. If this is the case, the total number of variants will be less than the sum of the other cells.

pathogenic likely pathogenic uncertain significance likely benign benign total
0 0 0 0 0 0

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.