Variants with conflicting interpretations "uncertain significance" from Personalized Diabetes Medicine Program, University of Maryland School of Medicine and "likely pathogenic" from any submitter

Minimum review status of the submission from Personalized Diabetes Medicine Program, University of Maryland School of Medicine:		Collection method of the submission from Personalized Diabetes Medicine Program, University of Maryland School of Medicine:
Minimum review status of the other submission:		Collection method of the other submission:
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 2

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_000545.8(HNF1A):c.616T>A (p.Trp206Arg)	rs1057524898
NM_175914.5(HNF4A):c.778G>T (p.Asp260Tyr)	rs1236613475

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.