|
rs10013040
|
|
|
0.010 |
GeneticVariation |
BEFREE |
For the other two NEIL3 SNPs (rs10013040 and rs1395479) and for the SNPs of OGG1 (rs1052133), APEX1 (rs1878703) and XRCC1 (rs25489) we observed no association with risk of myocardial infarction.
|
25703835 |
2015 |
|
rs1004467
|
|
A |
0.700 |
GeneticVariation |
GWASCAT |
A comprehensive 1,000 Genomes-based genome-wide association meta-analysis of coronary artery disease.
|
26343387 |
2015 |
|
rs1007888
|
|
|
0.010 |
GeneticVariation |
BEFREE |
However, the GG genotype of the MIF SNP rs1007888 was associated with MI in Czech female patients (p=0.027).
|
19167373 |
2009 |
|
rs1008563
|
|
|
0.010 |
GeneticVariation |
BEFREE |
Two IL8 SNPs (rs4073A/T, rs2227306C/T) and three SNPs tagging CXCR1 and CXCR2 (rs4674258C/T, rs1008563C/T, rs6723449T/C) were analyzed for association with IL8 levels and with MI risk.
|
24462138 |
2014 |
|
rs10116277
|
|
|
0.700 |
GeneticVariation |
GWASDB |
A common variant on chromosome 9p21 affects the risk of myocardial infarction.
|
17478679 |
2007 |
|
rs10118757
|
|
|
0.010 |
GeneticVariation |
BEFREE |
As reported previously, rs10118757 was not associated with MI in the current study.
|
23462334 |
2013 |
|
rs1012841819
|
|
|
0.010 |
GeneticVariation |
BEFREE |
We hypothesized that 3 nonsynonymous GRK4 single-nucleotide polymorphisms, R65L (rs2960306), A142V (rs1024323), and A486V (rs1801058), would be associated with blood pressure response to atenolol, but not hydrochlorothiazide, and would be associated with long-term cardiovascular outcomes (all-cause death, nonfatal myocardial infarction, nonfatal stroke) in participants treated with an atenolol-based versus verapamil-SR-based antihypertensive strategy.
|
22949529 |
2012 |
|
rs10176176
|
|
T |
0.700 |
GeneticVariation |
GWASCAT |
A comprehensive 1,000 Genomes-based genome-wide association meta-analysis of coronary artery disease.
|
26343387 |
2015 |
|
rs1024323
|
|
|
0.010 |
GeneticVariation |
BEFREE |
We hypothesized that 3 nonsynonymous GRK4 single-nucleotide polymorphisms, R65L (rs2960306), A142V (rs1024323), and A486V (rs1801058), would be associated with blood pressure response to atenolol, but not hydrochlorothiazide, and would be associated with long-term cardiovascular outcomes (all-cause death, nonfatal myocardial infarction, nonfatal stroke) in participants treated with an atenolol-based versus verapamil-SR-based antihypertensive strategy.
|
22949529 |
2012 |
|
rs1024611
|
|
|
0.020 |
GeneticVariation |
BEFREE |
In order to find new informative predictors of myocardial infarction, we performed an analysis of genotype frequencies of polymorphic markers of SELE (rs2076059, 3832T > C), SELP (rs6131, S290 N), SELL (rs1131498, F206L), ICAM1 (rs5498, K469E), VCAM1 (rs3917010, c.928 + 420A > C), PECAM1 (rs668, V125L), VEGFA (rs35569394, -2549(18)I/D), CCL2 (rs1024611, -2518A > G), NOS3 (rs1799983, E298D), and DDAH1 (rs669173, c.303 + 30998A > G) genes in the group of Russian men with myocardial infarction (N = 315) and the control group of corresponding ethnicity, gender, and age (N = 286).
|
26662939 |
2016 |
|
rs1024611
|
|
|
0.020 |
GeneticVariation |
BEFREE |
Emerging evidence has shown that the common polymorphism (-2518A>G; rs1024611) in the MCP-1 gene may contribute to the risk of MI, but individually published studies showed inconclusive results.
|
24053559 |
2013 |
|
rs10263017
|
|
|
0.700 |
GeneticVariation |
GWASDB |
Association of a polymorphism of BTN2A1 with myocardial infarction in East Asian populations.
|
21211798 |
2011 |
|
rs10281500
|
|
|
0.700 |
GeneticVariation |
GWASDB |
Association of a polymorphism of BTN2A1 with myocardial infarction in East Asian populations.
|
21211798 |
2011 |
|
rs10304
|
|
|
0.010 |
GeneticVariation |
BEFREE |
We confirmed that the haplotype constructed using rs5997872, rs56095120, rs9621187, and rs10304 is a useful genetic marker of MI in Japanese females.
|
22963604 |
2012 |
|
rs1041740
|
|
|
0.010 |
GeneticVariation |
BEFREE |
However, three variants were associated with increased risk of death from cardiovascular causes (sudden death, fatal myocardial infarction or stroke) during the follow-up: rs9974610 (HR 0.64, 95% CI 0.46-0.88, p=0.005), rs10432782 (HR 1.71, 95% CI 1.16-2.48, p=0.007) and rs1041740 (HR 1.78, 95% CI 1.10-2.78, p=0.02).
|
22608880 |
2012 |
|
rs1041981
|
|
|
0.720 |
GeneticVariation |
BEFREE |
Minor homozygous genotypes of polymorphisms in BAT1 (rs2239527, -23C/G), NFKBIL1 (rs2071592, -63T/A) and LTA (rs1800683, -162G/A; rs909253, 252G/A; rs1041981, Thr26Asn) were associated with moderately protective effects against myocardial infarction (P </= 0.045).
|
17517687 |
2007 |
|
rs1041981
|
|
|
0.720 |
GeneticVariation |
BEFREE |
A recent large-scale, genome-wide association study of single nucleotide polymorphisms showed a strong association between susceptibility to myocardial infarction and the Thr26Asn polymorphism in the lymphotoxin-alpha (LTA) gene.
|
15973460 |
2005 |
|
rs1041981
|
|
A |
0.720 |
SusceptibilityMutation |
CLINVAR |
|
|
|
|
rs1042034
|
|
|
0.010 |
GeneticVariation |
BEFREE |
Similarly, for the apolipoprotein B Asn4311Ser and Thr71Ile polymorphisms, genotypes associated with more adverse plasma apolipoprotein concentrations were associated with significantly lower risk of MI after adjustment for the apoB/apoA(1) ratio.
|
15256516 |
2004 |
|
rs1042522
|
|
|
0.010 |
GeneticVariation |
BEFREE |
We studied whether the NAMPT rs1319501, AKT1 rs3730358, p53 rs1042522, Mdm2 rs2279744 or eNOS rs1799983 SNP:s linked to NAMPT and Akt signaling associate with risk of myocardial infarction (MI).
|
22251423 |
2012 |
|
rs1042579
|
|
|
0.030 |
GeneticVariation |
BEFREE |
In a previous case control study of myocardial infarction (MI), we identified risk associated with the combination of two variants in the thrombomodulin (TM) gene (-1208-1209TTdelTT and A455V) and an interaction with increased body mass index (BMI).
|
15488871 |
2004 |
|
rs1042579
|
|
|
0.030 |
GeneticVariation |
BEFREE |
We investigated the relationship between polymorphisms in the Factor V (Leiden), prothrombin (20210 GgA) and thrombomodulin (Ala455Val) genes in patients with a myocardial infarction (MI) <45 years of age (n=195) and in unaffected siblings (n=107) and unrelated healthy race-matched individuals drawn from the same community (n=300).
|
14523329 |
2003 |
|
rs1042579
|
|
|
0.030 |
GeneticVariation |
BEFREE |
In this study, we examined the effects of 3 single-nucleotide polymorphisms (SNPs) in the TM gene (G-33A, C1418T and C1922T) on the development of myocardial infarction (MI) in Koreans.
|
12135317 |
2002 |
|
rs1042713
|
|
|
0.030 |
GeneticVariation |
BEFREE |
We focus on multimarker analyses and analyses of the effects of compound genotypes of two polymorphisms in the ADRB2 gene, rs1042713 and rs1042714, and 11 polymorphisms of the ACE gene, on the risk of such an aging-associated phenotype as myocardial infarction (MI).
|
20230274 |
2010 |
|
rs1042713
|
|
|
0.030 |
GeneticVariation |
BEFREE |
The Gln(27)Glu polymorphism but not the Arg(16)Gly polymorphism of the beta2-adrenergic receptor (ADRB2) gene appears to be associated with a broad range of aging-associated phenotypes, including cancers at different sites, myocardial infarction (MI), intermittent claudication (IC), and overall/healthy longevity in the Framingham Heart Study Offspring cohort.
|
20399803 |
2010 |