Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1799782
rs1799782
0.030 GeneticVariation BEFREE This meta-analysis suggested that TT genotype in the Arg194Trp polymorphism contributes to the CAD susceptibility, particularly in the Asian population. 28429350

2017

dbSNP: rs1799782
rs1799782
0.030 GeneticVariation BEFREE Subgroup analysis stratified by control source revealed associations between the Arg1</span>94Trp and Arg399Gln polymorphisms and su</span>sceptibility to CAD</span> under recessive and homozygous modes of inheritance, respectively. 27870881

2016

dbSNP: rs1799782
rs1799782
0.030 GeneticVariation BEFREE The adjusted risk of having CAD was more evident for rs1799782 (OR = 1.53; 95% CI: 1.16-2.02; P = 0.003), rs1801133 (OR = 1.54; 95% CI: 1.22-1.94; P < 0.001), and rs4846049 (OR = 1.74; 95% CI: 1.13-2.69; P = 0.013) under the recessive model. 24315498

2014