|
rs1217691063
|
|
|
0.070 |
GeneticVariation |
BEFREE |
Elevated Hcy levels in the presence of the T allele in the C677T gene and of the A allele in the A1298C gene are associated with AMI and massive and submassive PE.
|
29916259 |
2019 |
|
rs1217691063
|
|
|
0.070 |
GeneticVariation |
BEFREE |
This study compared genetic polymorphisms (factor V Leiden [FVL] 1691G/A, factor VII [FVII] 10976G/A, FVII HVR4, platelet membrane glycoproteins GP1BA 1018C/T, GP1BA VNTR, integrin ITGB3 1565T/C, ITGA2 807C/T and methylenetetrahydrofolate reductase [MTHFR] 677C/T), biochemical (fibrinogen and homocysteine), and conventional risk factors in 184 young and 166 elderly north Indian patients with acute myocardial infarction (AMI).
|
25155498 |
2016 |
|
rs1217691063
|
|
|
0.070 |
GeneticVariation |
BEFREE |
Such difference was due to a significantly higher frequency in AMI males of the MTHFR C677T variant homozygous genotype (O.R.3.05).
|
23171482 |
2012 |
|
rs1217691063
|
|
|
0.070 |
GeneticVariation |
BEFREE |
The aim of this study was to evaluate the association of prothrombotic gene polymorphisms [factor V Leiden (FVL) 1691GA, factor VII (FVII) 10976GA, FVII HVR4, platelet membrane glycoproteins GP1BA 1018CT, GP1BA VNTR, integrin ITGB3 1565TC, integrin ITGA2 807CT and methylenetetrahydrofolate reductase (MTHFR) 677C/T], plasma factors (fibrinogen and homocysteine) and traditional risk factors with acute myocardial infarction (AMI) in 184 patients ≤ 40 years of age and 350 controls (≤ 40 years) from north India.
|
22535530 |
2012 |
|
rs1217691063
|
|
|
0.070 |
GeneticVariation |
BEFREE |
Prevalence of MTHFR C677T mutant genotype was 49.1% (CT: 45.8%, TT: 3.3%) in controls and 48.45% (CT: 38.5%, TT: 9.95%) in patients with acute MI.
|
22222489 |
2011 |
|
rs1217691063
|
|
|
0.070 |
GeneticVariation |
BEFREE |
These data provide evidence for a major latent gene effect influencing variation in tHcy plasma levels, which is independent on C677T MTHFR polymorphism, and significantly affecting the risk of MI.
|
18223316 |
2008 |
|
rs1217691063
|
|
|
0.070 |
GeneticVariation |
BEFREE |
The methylenetetrahydrofolate reductase (MTHFR) 677C-->T mutation and cardiovascular risk--A case of ischemic stroke and acute myocardial infarction.
|
15773669 |
2005 |
|
rs699
|
|
|
0.040 |
GeneticVariation |
BEFREE |
There was a significant difference in the insertion deletion genotype distribution between two groups (P = 0.03) and a higher percentage of the T allele M235T polymorphism in the group of STEAMI patients (P = 0.02).
|
29474203 |
2018 |
|
rs699
|
|
|
0.040 |
GeneticVariation |
BEFREE |
The purpose of the present study was to assess whether the polymorphism of angiotensinogen (AGT) gene with threonine (T) instead of methionine (M) at amino acid 235 in exon 2 (M235T) had effects on cardiac remodelling after acute myocardial infarction.
|
23283822 |
2014 |
|
rs699
|
|
|
0.040 |
GeneticVariation |
BEFREE |
The angiotensinogen gene M235T polymorphism and acute myocardial infarction risk: a meta-analysis of 22 studies.
|
23666149 |
2013 |
|
rs699
|
|
|
0.040 |
GeneticVariation |
BEFREE |
The AGT M235T polymorphism associates with AMI risk and influences CAD severity.
|
20663844 |
2011 |
|
rs1799983
|
|
|
0.030 |
GeneticVariation |
BEFREE |
To investigate the association of allelic variants produced by the G894T transversion in eNOS (rs1799983) with post-AMI variables.
|
26002446 |
2015 |
|
rs1333049
|
|
|
0.030 |
GeneticVariation |
BEFREE |
Homozygous carriers of the rs1333049 C allele on chromosome 9p21 showed a reduced risk of 1 year ReMI in the contemporary percutaneous coronary intervention era, although the C allele had conferred susceptibility to their first AMI.
|
25232560 |
2014 |
|
rs1333049
|
|
|
0.030 |
GeneticVariation |
BEFREE |
For Pakistanis, the odds ratio for MI was 1.13 (95% CI, 1.05 to 1.22; P=2 x 10(-3)) for each copy of the C allele at rs1333049.
|
20395598 |
2010 |
|
rs1333049
|
|
|
0.030 |
GeneticVariation |
BEFREE |
This study examined the association of rs1333049 with myocardial infarction (MI), angiographic severity of CAD and clinical outcome after a first acute MI in Han Chinese.
|
19548844 |
2009 |
|
rs1799983
|
|
|
0.030 |
GeneticVariation |
BEFREE |
In contrast to previous reports, homozygosity for the Asp298 variant of the 894G>T polymorphism in the eNOS gene was not found to be associated with risk of AMI, extent of CAD and in-hospital mortality after AMI.
|
18495009 |
2008 |
|
rs1799983
|
|
|
0.030 |
GeneticVariation |
BEFREE |
Recent reports have suggested that the Glu298Asp polymorphism in exon 7 of the endothelial nitric oxide synthase gene is associated with coronary spasm and acute myocardial infarction.
|
12243851 |
2002 |
|
rs1076991
|
|
|
0.020 |
GeneticVariation |
BEFREE |
Similarly, low plasma glycine showed stronger risk relationship with AMI</span> in the rs1076991 CC genotype carriers but weaker associations in patients carrying the minor T allele (P<sub>interaction</sub>=0.02).
|
27872106 |
2016 |
|
rs1076991
|
|
|
0.020 |
GeneticVariation |
BEFREE |
We explored the association between a MTHFD1 polymorphism (rs1076991 C > T) and acute myocardial infarction (AMI), and potential effect modifications by folic acid/B12 and/or vitamin B6 treatment in suspected stable angina pectoris patients (n = 2381) participating in the randomized Western Norway B Vitamin Intervention Trial (WENBIT).
|
26803590 |
2016 |
|
rs1255283120
|
|
|
0.020 |
GeneticVariation |
BEFREE |
This study compared genetic polymorphisms (factor V Leiden [FVL] 1691G/A, factor VII [FVII] 10976G/A, FVII HVR4, platelet membrane glycoproteins GP1BA 1018C/T, GP1BA VNTR, integrin ITGB3 1565T/C, ITGA2 807C/T and methylenetetrahydrofolate reductase [MTHFR] 677C/T), biochemical (fibrinogen and homocysteine), and conventional risk factors in 184 young and 166 elderly north Indian patients with acute myocardial infarction (AMI).
|
25155498 |
2016 |
|
rs751377893
|
|
|
0.020 |
GeneticVariation |
BEFREE |
This study compared genetic polymorphisms (factor V Leiden [FVL] 1691G/A, factor VII [FVII] 10976G/A, FVII HVR4, platelet membrane glycoproteins GP1BA 1018C/T, GP1BA VNTR, integrin ITGB3 1565T/C, ITGA2 807C/T and methylenetetrahydrofolate reductase [MTHFR] 677C/T), biochemical (fibrinogen and homocysteine), and conventional risk factors in 184 young and 166 elderly north Indian patients with acute myocardial infarction (AMI).
|
25155498 |
2016 |
|
rs1042579
|
|
|
0.020 |
GeneticVariation |
BEFREE |
In conclusion, TM 1418C/T polymorphism is independent predictor of AMI and synergies with smoking.
|
22734102 |
2014 |
|
rs1255283120
|
|
|
0.020 |
GeneticVariation |
BEFREE |
Multinominal logistic-regression analysis showed gene-gene (GP1BA 1018C/T with GP1BA VNTR and ITGA2 807C/T with ITGB3 1565T/C polymorphisms) and gene-environment interactions (gene polymorphisms with smoking) operating in the occurrence of AMI in young.
|
22535530 |
2012 |
|
rs899127658
|
|
|
0.020 |
GeneticVariation |
BEFREE |
Analysis of polymorphisms Leiden Factor V G1691A and prothrombin G20210A as risk factors for acute myocardial infarction.
|
21918818 |
2011 |
|
rs1801253
|
|
|
0.020 |
GeneticVariation |
BEFREE |
We investigated the possible association between the Arg389Gly polymorphism and LVH among non-diabetic and diabetic acute myocardial infarction (AMI) survivors.
|
20731869 |
2010 |