List of variants in gene HNF1B reported as likely benign by GeneDx

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: 21

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_000458.4(HNF1B):c.1535-188C>T	rs75148877	0.01577
NM_000458.4(HNF1B):c.1340-303T>A	rs112298654	0.01150
NM_000458.4(HNF1B):c.1207-66G>A	rs114224174	0.00644
NM_000458.4(HNF1B):c.1535-44G>C	rs10083829	0.00552
NM_000458.3(HNF1B):c.-178G>A	rs148442901	0.00528
NM_000458.4(HNF1B):c.1207-54G>A	rs138615516	0.00456
NM_000458.4(HNF1B):c.344+196C>A	rs376100923	0.00391
NM_000458.4(HNF1B):c.810-32T>C	rs752563696	0.00384
NM_000458.4(HNF1B):c.344+198T>G	rs373107533	0.00344
NM_000458.4(HNF1B):c.1413C>T (p.Pro471=)	rs140781855	0.00325
NM_000458.4(HNF1B):c.444G>A (p.Ser148=)	rs147218489	0.00228
NM_000458.4(HNF1B):c.951C>G (p.Ala317=)	rs145750370	0.00127
NM_000458.4(HNF1B):c.1045+12T>C	rs141166864	0.00097
NM_000458.4(HNF1B):c.948C>T (p.Asp316=)	rs373132003	0.00006
NM_000458.4(HNF1B):c.231C>G (p.Asp77Glu)	rs760448993	0.00001
NM_000458.4(HNF1B):c.983C>T (p.Pro328Leu)	rs764132839	0.00001
NM_000458.4(HNF1B):c.-27A>C	rs1402766102
NM_000458.4(HNF1B):c.-31C>G	rs771697321
NM_000458.4(HNF1B):c.1474G>A (p.Gly492Ser)
NM_000458.4(HNF1B):c.1654-14CT[4]	rs886052890
NM_000458.4(HNF1B):c.182T>G (p.Val61Gly)

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.