ClinVar Miner

List of variants in gene RINT1 reported as uncertain significance for PTEN hamartoma tumor syndrome

Included ClinVar conditions (20):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 2
Download table as spreadsheet
NM_021930.6(RINT1):c.1447A>G (p.Met483Val) rs869312982
NM_021930.6(RINT1):c.1671_1671+2del rs869312981

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.