Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs17576
rs17576
0.020 GeneticVariation BEFREE C1562T and R279Q polymorphisms are associated with the susceptibility to premature MI, but cannot predict long-term cardiac events in these patients. 28453874

2018

dbSNP: rs3918242
rs3918242
0.020 GeneticVariation BEFREE Moreover, we also found that there is a statistically significant association between rs3918242 polymorphism and myocardial infarction (MI) in Asians with allelic model (OR 1.66; 95% CI 1.29-2.14; <i>p</i> < 0.0001), recessive model (OR 2.29; 95% CI 1.44-3.63; <i>p</i> = 0.004), and dominant (OR 1.74; 95% CI 1.29-2.35; <i>p</i> = 0.0003) model. 29507703

2018

dbSNP: rs3918242
rs3918242
0.020 GeneticVariation BEFREE Multiple logistic analysis was performed between MI patients and controls to estimate the risk, and after adjusting for identified risk factors, the CT + TT genotypes of MMP9 rs3918242 were found to be significantly associated with increased risk of developing MI than those with the CC genotype (OR = 2.88, P < 0.01). 26985929

2016

dbSNP: rs17576
rs17576
0.020 GeneticVariation BEFREE The -1562C>T or R2</span>79Q polymorphism of MMP-9 gene and smoking have a synergistic effect and are significantly associated with the risk of MI in Chinese Uighur population, respectively. 21733941

2012