Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1884614
rs1884614
0.090 GeneticVariation BEFREE However, the frequency of haplotype, CCTA, built by rs4810424, rs1884613, rs1884614 and rs2144908 was significantly higher in the type 2 diabetes mellitus group compared with the control group (χ2=8.34, P=0.004). 26781905

2016

dbSNP: rs1884614
rs1884614
0.090 GeneticVariation BEFREE In the case-control analysis, PPARG rs1801282 (Pro12Ala) (OR=1.48 (1.02-2.16)), ADIPOQ rs1063539 (OR=1.17 (1.01-1.35)), and HNF4A rs1884614 (OR=1.16 (1.00-1.32) were associated with T2D (P(allelic)<0.05). 22515931

2012

dbSNP: rs1884614
rs1884614
0.090 GeneticVariation BEFREE Minor allele frequency of rs1884614 and rs2071197 was significantly lower in early onset T2DM when compared to NGT subjects (p < 0.01). 21062274

2011

dbSNP: rs1884614
rs1884614
0.090 GeneticVariation BEFREE To summarize, our investigation did not confirm the effects of HNF4A variants (rs1884614 and rs2425637) on T2D risk, but found that the risk HNF4A contributed to T2D might be population specific. 20558840

2010

dbSNP: rs1884614
rs1884614
0.090 GeneticVariation BEFREE SNP rs1884614 in the P2 promoter region of the HNF-4alpha gene may influence insulin secretion in non-obese Japanese subjects with type 2 diabetes. 18654034

2008

dbSNP: rs1884614
rs1884614
0.090 GeneticVariation BEFREE This study was aimed to assess the association of the two single nucleotide polymorphisms (SNPs) near P2 promoter (rs1884614 and rs2144908) of hepatocyte nuclear factor-4alpha (HNF4A) with insulin secretion index and type 2 diabetes in Thais. 17805472

2007

dbSNP: rs1884614
rs1884614
0.090 GeneticVariation BEFREE The risk allele of the rs1884614, which is located 4 kb upstream of the HNF4A P2 promoter, was associated with type 2 diabetes (odds ratio [OR]=1.14, p=0.02) and with a subtle increase in post-OGTT plasma glucose levels in glucose-tolerant subjects (additive model, p=0.05). 15735891

2005

dbSNP: rs1884614
rs1884614
0.090 GeneticVariation BEFREE In the P2 promoter, the htSNP rs1884614 showed borderline association with both type 2 diabetes (OR 1.40, P = 0.09) and the combined type 2 diabetes/IGT trait (1.35, P = 0.07). 15561969

2004

dbSNP: rs1884614
rs1884614
0.090 GeneticVariation BEFREE Testing of additional SNPs 5' of rs1884614 revealed a >10-kb haplotype block that was associated with type 2 diabetes. 15047632

2004