Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1052133
rs1052133
OGG1 ; CAMK1
0.020 GeneticVariation BEFREE In addition, we confirmed the association of XRCC3 Thr241Met and hOGG1 Ser326Cys gene variants with CAD by haplotype analysis. 23368530

2013
dbSNP: rs1052133
rs1052133
OGG1 ; CAMK1
0.020 GeneticVariation BEFREE We found that presence of the hOGG1 Ser</span>(326)Cys polymorphism was associated with a significantly increased risk of CAD and multi-vessel disease when assuming a dominant model of inheritance (OR: 1.52 [95%:1.082~2.133], p=0.015; OR: 2.26 [95%:1.232~4.156], p=0.007). 20667409

2010