HNF4A, hepatocyte nuclear factor 4 alpha, 3172

N. diseases: 340; N. variants: 74
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X
0.060 GeneticVariation disease BEFREE In SNP rs1884613 of HNF4A, subjects with the C allele carried a 1.31- and 1.50-times higher risk of developing MetS and TD, respectively, compared to those with the G allele, after adjusting for potential covariates. 30415809 2018
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X
0.060 GeneticVariation disease BEFREE Our study demonstrates that HNF4α genetic variants are associated with the MetS and metabolic parameters in French Canadian children and adolescents. 25671620 2015
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X
0.060 Biomarker disease BEFREE Nine HNF4 alpha SNPs were genotyped in 390 type 2 diabetic subjects with metabolic syndrome, 135 type 2 diabetic subjects without metabolic syndrome, and 160 control subjects. 21983932 2012
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X
0.060 Biomarker disease BEFREE From 322 with clinically labeled type 2 diabetes, we sequenced HNF1A and HNF4A in 80 with diabetes diagnosed ≤ 30 years and/or diabetes diagnosed ≤ 45 years without metabolic syndrome. 22432108 2012
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X
0.060 GeneticVariation disease BEFREE Nine SNPs spanning the HNF4 alpha P2 promoter (rs4810424, rs1884613 and rs1884614) and coding region (rs2144908, rs6031551, rs6031552, rs1885088, rs1028583 and rs3818247) were genotyped in 160 subjects without diabetes or metabolic syndrome. 21633728 2011
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X
0.060 GeneticVariation disease BEFREE In conclusion, we show for the first time that common HNF4A variants are associated with high serum lipid levels and the metabolic syndrome. 16804065 2006