ClinVar Miner

List of variants reported as likely benign for chronic kidney disease

Included ClinVar conditions (1):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 4
Download table as spreadsheet
NM_000091.4(COL4A3):c.346C>A (p.Pro116Thr) rs115324397
NM_000204.4(CFI):c.782G>A (p.Gly261Asp) rs112534524
NM_022489.4(INF2):c.3221G>A (p.Arg1074Lys) rs201445955
NM_024753.5(TTC21B):c.3004C>G (p.Leu1002Val) rs146496725

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.