ClinVar Miner

List of variants in gene HNF1B reported as likely benign for abdominal and pelvic region disorder

Included ClinVar conditions (902):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 20
Download table as spreadsheet
NM_000458.3(HNF1B):c.-178G>A rs148442901
NM_000458.3(HNF1B):c.-232C>T rs142612536
NM_000458.4(HNF1B):c.*403A>G rs557216745
NM_000458.4(HNF1B):c.*445A>G rs571607314
NM_000458.4(HNF1B):c.*683G>A rs144234352
NM_000458.4(HNF1B):c.*804T>C rs75361710
NM_000458.4(HNF1B):c.*938A>G rs574000398
NM_000458.4(HNF1B):c.-67C>T rs140699244
NM_000458.4(HNF1B):c.1045+12T>C rs141166864
NM_000458.4(HNF1B):c.1413C>T (p.Pro471=) rs140781855
NM_000458.4(HNF1B):c.1474G>A (p.Gly492Ser) rs187556368
NM_000458.4(HNF1B):c.226G>T (p.Gly76Cys) rs144425830
NM_000458.4(HNF1B):c.244G>A (p.Asp82Asn) rs140562402
NM_000458.4(HNF1B):c.444G>A (p.Ser148=) rs147218489
NM_000458.4(HNF1B):c.684C>G (p.Asn228Lys) rs202151409
NM_000458.4(HNF1B):c.708C>T (p.Phe236=)
NM_000458.4(HNF1B):c.73G>T (p.Val25Leu) rs139107479
NM_000458.4(HNF1B):c.750C>T (p.Tyr250=) rs144249535
NM_000458.4(HNF1B):c.951C>G (p.Ala317=) rs145750370

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.