Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1052133
rs1052133
0.050 GeneticVariation BEFREE Evidence suggests that Ser326Cys, a genetic polymorphism of human 8-oxoguanine glycosylase 1 (hOGG1), is associated with insulin resistance and type 2 diabetes; however, the underlying mechanism is unclear. 24998955

2014

dbSNP: rs1052133
rs1052133
0.050 GeneticVariation BEFREE According to our study results, it has been observed that the combined evaluation of GSTM1-GSTT1-GSTP1 and OGG1 Ser326Cys gene polymorphisms can be used as candidate genes in the etiology of T2DM, especially in the development of T2DM. 22652274

2012

dbSNP: rs1052133
rs1052133
0.050 GeneticVariation BEFREE Furthermore, a significantly increased risk of T2DM was observed in the subjects carrying heterozygous variant of c.-23A>G and homozygous mutation of Ser326Cys (OR=3.684, 95%CI=1.400-9.697). 20562008

2010

dbSNP: rs1052133
rs1052133
0.050 GeneticVariation BEFREE Of the SNPs examined for association, the Ser(326)Cys (rs1052133) exhibited significant association with T2DM (</span>p = 0.016) after accounting for age and sex effects. 20606456

2010

dbSNP: rs1052133
rs1052133
0.050 GeneticVariation BEFREE The association of the Ser326Cys polymorphism of the 8-oxoguanine glycosylase 1 (OGG1) gene with type 2 diabetes was examined using a Japanese population (n (M/W): 4585 (2085/2500); age: 62.6 +/- 10.9 years). 19486888

2009

dbSNP: rs1801126
rs1801126
0.010 GeneticVariation BEFREE In this study, we screened for the polymorphism variants Val83Met (c.247G>A, rs4866) in hMTH1; c.-53G>C (rs56387615), c.-23A>G (rs1801129) and c.-18G>T (rs1801126) in the 5'-UTR of hOGG1; and AluYb8 insertion in MUTYH (AluYb8MUTYH, rs10527342) and investigated their synergistic effect on the risk of T2DM in the Chinese population. 23396182

2013

dbSNP: rs1801129
rs1801129
0.010 GeneticVariation BEFREE In this study, we screened for the polymorphism variants Val83Met (c.247G>A, rs4866) in hMTH1; c.-53G>C (rs56387615), c.-23A>G (rs1801129) and c.-18G>T (rs1801126) in the 5'-UTR of hOGG1; and AluYb8 insertion in MUTYH (AluYb8MUTYH, rs10527342) and investigated their synergistic effect on the risk of T2DM in the Chinese population. 23396182

2013

dbSNP: rs56387615
rs56387615
0.010 GeneticVariation BEFREE In this study, we screened for the polymorphism variants Val83Met (c.247G>A, rs4866) in hMTH1; c.-53G>C (rs56387615), c.-23A>G (rs1801129) and c.-18G>T (rs1801126) in the 5'-UTR of hOGG1; and AluYb8 insertion in MUTYH (AluYb8MUTYH, rs10527342) and investigated their synergistic effect on the risk of T2DM in the Chinese population. 23396182

2013

dbSNP: rs2072668
rs2072668
0.010 GeneticVariation BEFREE Another intronic variant (rs2072668), which was in strong linkage disequilibrium (r(2) = 0.96) with Ser(326)Cys also exhibited significant association with T2DM (p = 0.031). 20606456

2010