HNF1A, HNF1 homeobox A, 6927

N. diseases: 292; N. variants: 105
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0028754
Disease: Obesity
Obesity
0.160 GeneticVariation disease BEFREE We analysed the interaction between HNF1A rs7957197 and weight-loss diets with regard to weight loss and insulin resistance improvement among 722 overweight/obese adults from a 2-year randomized weight-loss trial, the POUNDS Lost trial. 29424957 2018
CUI: C0028754
Disease: Obesity
Obesity
0.160 GeneticVariation disease BEFREE According to our preliminary findings, genetic variation in the INSR and HNF1A genes may differentially affect weight loss in obese individuals treated with topiramate and genes related to insulin action are implicated in modulating topiramate response. 26524290 2016
CUI: C0028754
Disease: Obesity
Obesity
0.160 GeneticVariation disease BEFREE Further, HNF1A genotypes interact with obesity to set CRP level, revealing that genetic determinants for CRP level may be different between obese and non-obese individuals. 21195701 2011
CUI: C0028754
Disease: Obesity
Obesity
0.160 Biomarker disease BEFREE The patient, who presented with apparent type 2 diabetes, had concomitant MODY 3, inherited from his mother's side, and some features of type 2 diabetes secondary to marked obesity. 18036134 2008
CUI: C0028754
Disease: Obesity
Obesity
0.160 GeneticVariation disease BEFREE Analysis of statistically similar SNPs suggested that the causative variants for systolic blood pressure were located in F11R, whilst those for central obesity could be due to causative variants in the transcription factor 1 gene immediately upstream. 18067551 2008
CUI: C0028754
Disease: Obesity
Obesity
0.160 GeneticVariation disease BEFREE The findings also show that HNF1A mutations can be associated with typical adult-onset insulin-resistant obesity-related diabetes in addition to maturity-onset diabetes of the young. 11904371 2002
CUI: C0028754
Disease: Obesity
Obesity
0.160 Biomarker disease HPO