ClinVar Miner

Submissions for variant NM_000545.6(HNF1A):c.1722C>A (p.Gly574=) (rs141304623)

Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
Download table as spreadsheet
Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Personalized Diabetes Medicine Program,University of Maryland School of Medicine RCV000445514 SCV000537090 likely benign Monogenic diabetes 2015-11-10 criteria provided, single submitter research ACMG Criteria: PP3, BS2 (, BP4
Athena Diagnostics Inc RCV000713789 SCV000844421 benign not provided 2018-03-05 criteria provided, single submitter clinical testing

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.