|
rs1800562
|
|
|
0.010 |
GeneticVariation |
BEFREE |
Increased risk of acute myocardial infarction in carriers of the hemochromatosis gene Cys282Tyr mutation : a prospective cohort study in men in eastern Finland.
|
10491370 |
1999 |
|
rs6313
|
|
|
0.020 |
GeneticVariation |
BEFREE |
The association of T102C polymorphism of the 5-HT2A receptor gene with non-fatal AMI was statistically significant and independent of other risk factors in males.
|
10781645 |
2000 |
|
rs1613662
|
|
|
0.010 |
GeneticVariation |
BEFREE |
The contribution of the T13254C dimorphism, which predicted the substitution of serine 219 by proline, to risk of MI was assessed in 525 patients with acute MI and 474 controls, all aged <75 years.
|
11571236 |
2001 |
|
rs201058276
|
|
|
0.020 |
GeneticVariation |
BEFREE |
In order to determine the role of two polymorphisms in the factor VII gene (R353Q and intron 7 hypervariable region) in the susceptibility to develop early myocardial infarction, a total of 175 patients with acute myocardial infarction aged 50 years or less (mean age 41+/-7 years) and 200 controls (average age 42+/-6) without cardiovascular disease were genotyped for these polymorphisms.
|
11578716 |
2001 |
|
rs1800730
|
|
|
0.010 |
GeneticVariation |
BEFREE |
To test whether genetic haemochromatosis is associated with myocardial infarction, we determined the prevalence of three mutations in the HFE gene (Cys282Tyr, His63Asp and Ser65Cys) in a 2 : 1 case-control study including 177 patients who survived an acute myocardial infarction and 89 controls.
|
11886425 |
2002 |
|
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 |
|
rs201058276
|
|
|
0.020 |
GeneticVariation |
BEFREE |
Associations of the known polymorphisms of the coagulation factor VII (FVII) gene (R353Q), the coagulation factor XIII (FXIII) gene (V34L) and the glycoprotein Ia (Gp1a) gene (C807T) with the occurrence of AMI were studied in 142 AMI survivors and 142 age- and sex-matched control subjects.
|
12486862 |
2002 |
|
rs1183027238
|
|
|
0.010 |
GeneticVariation |
BEFREE |
Associations of the known polymorphisms of the coagulation factor VII (FVII) gene (R353Q), the coagulation factor XIII (FXIII) gene (V34L) and the glycoprotein Ia (Gp1a) gene (C807T) with the occurrence of AMI were studied in 142 AMI survivors and 142 age- and sex-matched control subjects.
|
12486862 |
2002 |
|
rs200478651
|
|
|
0.010 |
GeneticVariation |
BEFREE |
Associations of the known polymorphisms of the coagulation factor VII (FVII) gene (R353Q), the coagulation factor XIII (FXIII) gene (V34L) and the glycoprotein Ia (Gp1a) gene (C807T) with the occurrence of AMI were studied in 142 AMI survivors and 142 age- and sex-matched control subjects.
|
12486862 |
2002 |
|
rs1801253
|
|
|
0.020 |
GeneticVariation |
BEFREE |
Our findings suggest that the genotype of Arg389Gly polymorphism in the human ADRB1 gene is associated with AMI.
|
12851615 |
2003 |
|
rs1042579
|
|
|
0.020 |
GeneticVariation |
BEFREE |
Despite the fact that TM promoter G-33A and C1418T polymorphisms are common in the Chinese population, the association between G-33A mutation and premature AMI indicates that we must focus on promoter G-33A polymorphism rather than C1418T polymorphism in terms of the role of TM gene mutation on premature AMI.
|
14715348 |
2004 |
|
rs1131012
|
|
|
0.010 |
GeneticVariation |
BEFREE |
The frequency of the Gly670Arg polymorphism was significantly higher in patients with AMI (58.9% vs. 48.3%; P = 0.019), whereas the frequencies of the other two SNPs (Leu125Val and Ser563Asn) were not significantly different between patients and controls.
|
15265022 |
2004 |
|
rs12953
|
|
|
0.010 |
GeneticVariation |
BEFREE |
The frequency of the Gly670Arg polymorphism was significantly higher in patients with AMI (58.9% vs. 48.3%; P = 0.019), whereas the frequencies of the other two SNPs (Leu125Val and Ser563Asn) were not significantly different between patients and controls.
|
15265022 |
2004 |
|
rs281865545
|
|
|
0.010 |
GeneticVariation |
BEFREE |
The frequency of the Gly670Arg polymorphism was significantly higher in patients with AMI (58.9% vs. 48.3%; P = 0.019), whereas the frequencies of the other two SNPs (Leu125Val and Ser563Asn) were not significantly different between patients and controls.
|
15265022 |
2004 |
|
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 |
|
rs1064039
|
|
|
0.010 |
GeneticVariation |
BEFREE |
Cystatin C levels are decreased in acute myocardial infarction: effect of cystatin C G73A gene polymorphism on plasma levels.
|
15882666 |
2005 |
|
rs28940578
|
|
|
0.010 |
GeneticVariation |
BEFREE |
To evaluate whether inflammatory alleles of pyrin, the gene responsible for familial Mediterranean fever (FMF) may play an opposite role in CHD and in longevity, we examined three FMF-associated mutations, M694V (A2080G), M694I (G2082A), and V726A (T2177C), encoded by the FMF gene (MEFV) in 121 patients affected by acute myocardial infarction (AMI), in 68 centenarians, and in 196 age-matched controls from Sicily.
|
16387839 |
2006 |
|
rs28940579
|
|
|
0.010 |
GeneticVariation |
BEFREE |
To evaluate whether inflammatory alleles of pyrin, the gene responsible for familial Mediterranean fever (FMF) may play an opposite role in CHD and in longevity, we examined three FMF-associated mutations, M694V (A2080G), M694I (G2082A), and V726A (T2177C), encoded by the FMF gene (MEFV) in 121 patients affected by acute myocardial infarction (AMI), in 68 centenarians, and in 196 age-matched controls from Sicily.
|
16387839 |
2006 |
|
rs61752717
|
|
|
0.010 |
GeneticVariation |
BEFREE |
After adjustment for well-recognized AMI risk factors, the M694V allele still predicted a significant risk to develop AMI.
|
16387839 |
2006 |
|
rs63751001
|
|
|
0.010 |
GeneticVariation |
BEFREE |
A 16-year-old survivor of acute myocardial infarction with 3-vessel coronary artery disease exhibited compound heterozygosity for the well-known nonsense mutation (c.3421C>T; R1141X) in exon 24 and a novel missense mutation (c.3662G>A; R1221H) in exon 26 of the ABCC6 gene.
|
16854481 |
2007 |
|
rs72653706
|
|
|
0.010 |
GeneticVariation |
BEFREE |
A 16-year-old survivor of acute myocardial infarction with 3-vessel coronary artery disease exhibited compound heterozygosity for the well-known nonsense mutation (c.3421C>T; R1141X) in exon 24 and a novel missense mutation (c.3662G>A; R1221H) in exon 26 of the ABCC6 gene.
|
16854481 |
2007 |
|
rs1053874
|
|
|
0.010 |
GeneticVariation |
BEFREE |
Our data demonstrate that Gln222Arg polymorphism in the DNase I gene is associated with MI in the Japanese patients.
|
16877481 |
2006 |
|
rs34637584
|
|
|
0.010 |
GeneticVariation |
BEFREE |
Five LRRK2 G2019S carriers were identified, of whom 4 had Parkinson disease (clinically and pathologically confirmed), and the fifth was a control subject who died at age 68 years after an acute myocardial infarction with no evidence of neurodegenerative abnormalities.
|
16966501 |
2006 |
|
rs1217035505
|
|
|
0.010 |
GeneticVariation |
BEFREE |
The common Ala-87-Thr polymorphism of the P2Y11 receptor is associated with AMI and increased levels of C-reactive protein.
|
17135283 |
2007 |
|
rs3745601
|
|
|
0.010 |
GeneticVariation |
BEFREE |
The common Ala-87-Thr polymorphism of the P2Y11 receptor is associated with AMI and increased levels of C-reactive protein.
|
17135283 |
2007 |