rs1805087, MTR

N. diseases: 135
Disease: Myocardial Infarction ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Myocardial Infarction
CUI: C0027051
Disease: Myocardial Infarction
0.050 GeneticVariation BEFREE The results of combined analyses of the MTR A2756G polymorphism suggested that the G allele was associated with increased risk of CHD and myocardial infarction (MI) especially for Europeans (GG vs. AA for CHD: OR [95% CI]=1.63 [1.18-2.25], p(z)(-test)=0.001, p(heterogeneity)=0.274; GG+AG vs. AA for MI: OR [95% CI]=1.44 [1.08-1.93], p(z)(-test)=0.014, p(heterogeneity)=0.611). 21780915 2012
Myocardial Infarction
CUI: C0027051
Disease: Myocardial Infarction
0.050 GeneticVariation BEFREE The present study showed a significant but not independent association between the 2756A>G polymorphism of the MTR (presence of G allele) and MI in the Tunisian population. 18844488 2008
Myocardial Infarction
CUI: C0027051
Disease: Myocardial Infarction
0.050 GeneticVariation BEFREE We examined whether C677T methylenetetrahydrofolate reductase and A2756G methionine synthase polymorphisms could affect the relative risk for MI. 15820491 2005
Myocardial Infarction
CUI: C0027051
Disease: Myocardial Infarction
0.050 GeneticVariation BEFREE Influence of a methionine synthase (D919G) polymorphism on plasma homocysteine and folate levels and relation to risk of myocardial infarction. 11257268 2001
Myocardial Infarction
CUI: C0027051
Disease: Myocardial Infarction
0.050 GeneticVariation BEFREE The G allele of MS A2756G yields an OR of 0.92(95% CI 0.47-1.81) for IS and 1.17 (95% CI 0.58-2.37) for MI. 11672761 2001