List of variants in gene HNF1A reported as benign for Monogenic diabetes

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 10

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_000545.8(HNF1A):c.1720A>G (p.Ser574Gly)	rs1169305	0.98610
NM_000545.8(HNF1A):c.293C>T (p.Ala98Val)	rs1800574	0.02065
NM_000545.8(HNF1A):c.92G>A (p.Gly31Asp)	rs137853247	0.00076
NM_000545.8(HNF1A):c.185A>G (p.Asn62Ser)	rs377129682	0.00010
NM_000545.8(HNF1A):c.225C>T (p.Asp75=)	rs202180554	0.00009
NM_000545.8(HNF1A):c.1522G>A (p.Glu508Lys)	rs483353044	0.00003
NM_000545.8(HNF1A):c.-167TGGGGGT[3]	rs538476099
NM_000545.8(HNF1A):c.1135C>G (p.Pro379Ala)	rs754729248
NM_000545.8(HNF1A):c.1136C>A (p.Pro379His)	rs371717826
NM_000545.8(HNF1A):c.155_156delinsCT (p.Gly52Ala)	rs587778393

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.