Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs17576
rs17576
0.030 GeneticVariation BEFREE The meta-analysis of the R279Q polymorphism, including 6 studies with 6,983 cases and 3,282 controls, showed that the R279Q polymorphism was not associated with CHD (p = 0.16). 23328249

2013

dbSNP: rs17576
rs17576
0.030 GeneticVariation BEFREE This meta-analysis provided evidence that genetic polymorphism of MMP1-1607 1G/2G, MMP3-Gly45lys, MMP3-376 G/C, MMP3-1171 5A/6A, MMP9-1562 C/T and MMP9-R279Q have a small to medium effect on incidence of coronary disease. 22226810

2012

dbSNP: rs17576
rs17576
0.030 GeneticVariation BEFREE The aim of this study was to analyze the occurrence of the -1612 5A/6A, -376C/G, and Glu45Lys polymorphisms of MMP3 and the -1562C/T and R279Q polymorphisms of MMP9 and their relation to the risk of coronary heart disease (CHD; stenosis >/=50% of the diameter in at least one major coronary artery) in a Chinese Han population. 19438845

2009

dbSNP: rs3918242
rs3918242
0.020 GeneticVariation BEFREE MMP9 rs3918242 TT genotype is associated with elevated serum TG and LDL-C, and enhanced LDL-C-lowering response upon simvastatin treatment in Chinese patients with CHD. 28390432

2017

dbSNP: rs3918242
rs3918242
0.020 GeneticVariation BEFREE We observed that the T allele of rs3918242 was correlated with increased risk of coron</span>ary artery disease (OR = 1.88, 95%CI = 1.39-2.55). 27323016

2016