|
rs646776
|
|
|
0.810 |
GeneticVariation |
BEFREE |
Three SNPs 12740374 G/T, rs599839A/G and rs646776T/C mapping at 1p13 were analysed for association with serum lipid levels and the risk of MI by a weighted least square regression and logistic regression analyses, respectively.
|
23067240 |
2012 |
|
rs11206510
|
|
T |
0.810 |
GeneticVariation |
GWASCAT |
Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants.
|
19198609 |
2009 |
|
rs11206510
|
|
T |
0.810 |
GeneticVariation |
GWASDB |
Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants.
|
19198609 |
2009 |
|
rs1122608
|
|
G |
0.810 |
GeneticVariation |
GWASDB |
Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants.
|
19198609 |
2009 |
|
rs1122608
|
|
G |
0.810 |
GeneticVariation |
GWASCAT |
Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants.
|
19198609 |
2009 |
|
rs646776
|
|
T |
0.810 |
GeneticVariation |
GWASCAT |
Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants.
|
19198609 |
2009 |
|
rs646776
|
|
T |
0.810 |
GeneticVariation |
GWASDB |
Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants.
|
19198609 |
2009 |
|
rs10738607
|
|
|
0.810 |
GeneticVariation |
GWASDB |
A common variant on chromosome 9p21 affects the risk of myocardial infarction.
|
17478679 |
2007 |
|
rs3803915
|
|
C |
0.800 |
GeneticVariation |
GWASCAT |
Our study identified two novel susceptibility loci for MI: PLCL2 on chromosome 3p24.3 (rs4618210:A>G, P = 2.60 × 10(-9), odds ratio (OR) = 0.91) and AP3D1-DOT1L-SF3A2 on chromosome 19p13.3 (rs3803915:A>C, P = 3.84 × 10(-9), OR = 0.89).
|
24916648 |
2015 |
|
rs3803915
|
|
C |
0.800 |
GeneticVariation |
GWASDB |
Our study identified two novel susceptibility loci for MI: PLCL2 on chromosome 3p24.3 (rs4618210:A>G, P = 2.60 × 10(-9), odds ratio (OR) = 0.91) and AP3D1-DOT1L-SF3A2 on chromosome 19p13.3 (rs3803915:A>C, P = 3.84 × 10(-9), OR = 0.89).
|
24916648 |
2015 |
|
rs4618210
|
|
G |
0.800 |
GeneticVariation |
GWASCAT |
Our study identified two novel susceptibility loci for MI: PLCL2 on chromosome 3p24.3 (rs4618210:A>G, P = 2.60 × 10(-9), odds ratio (OR) = 0.91) and AP3D1-DOT1L-SF3A2 on chromosome 19p13.3 (rs3803915:A>C, P = 3.84 × 10(-9), OR = 0.89).
|
24916648 |
2015 |
|
rs4618210
|
|
G |
0.800 |
GeneticVariation |
GWASDB |
Our study identified two novel susceptibility loci for MI: PLCL2 on chromosome 3p24.3 (rs4618210:A>G, P = 2.60 × 10(-9), odds ratio (OR) = 0.91) and AP3D1-DOT1L-SF3A2 on chromosome 19p13.3 (rs3803915:A>C, P = 3.84 × 10(-9), OR = 0.89).
|
24916648 |
2015 |
|
rs11748327
|
|
|
0.800 |
GeneticVariation |
GWASDB |
SNPs on chromosome 5p15.3 associated with myocardial infarction in Japanese population.
|
21107343 |
2011 |
|
rs11748327
|
|
|
0.800 |
GeneticVariation |
GWASCAT |
SNPs on chromosome 5p15.3 associated with myocardial infarction in Japanese population.
|
21107343 |
2011 |
|
rs1746048
|
|
C |
0.800 |
GeneticVariation |
GWASDB |
Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants.
|
19198609 |
2009 |
|
rs1746048
|
|
C |
0.800 |
GeneticVariation |
GWASCAT |
Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants.
|
19198609 |
2009 |
|
rs6725887
|
|
C |
0.800 |
GeneticVariation |
GWASCAT |
Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants.
|
19198609 |
2009 |
|
rs6725887
|
|
C |
0.800 |
GeneticVariation |
GWASDB |
Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants.
|
19198609 |
2009 |
|
rs6929846
|
|
|
0.780 |
GeneticVariation |
BEFREE |
We have previously shown that the C→T polymorphism (rs6929846) of the butyrophilin, subfamily 2, member A1 gene (BTN2A1) was significantly associated with myocardial infarction.
|
24452779 |
2014 |
|
rs6929846
|
|
|
0.780 |
GeneticVariation |
BEFREE |
Multivariable logistic regression analyses with adjustment for covariates revealed that rs6929846 of BTN2A1 was significantly associated with MI in individuals with (P=0.0001; odds ratio, 1.49) or without (P=1.6x10-7; odds ratio, 2.32) hypertension; in individuals with (P=0.0002; odds ratio, 1.65) or without (P=8.1x10-7; odds ratio, 1.76) DM; and in individuals without CKD (P=6.0x10-11; odds ratio, 2.03), but not in those with CKD.
|
21347509 |
2011 |
|
rs6929846
|
|
|
0.780 |
GeneticVariation |
BEFREE |
Given that diabetes mellitus is an important risk factor for myocardial infarction, the association of rs6929846 of BTN2A1 with myocardial infarction might be attributable, at least in part, to its effect on susceptibility to diabetes.
|
21672009 |
2011 |
|
rs6929846
|
|
|
0.780 |
GeneticVariation |
BEFREE |
Given that metabolic syndrome (MetS) is an important risk factor for myocardial infarction, the association of the rs6929846 of BTN2A1 with myocardial infarction</span> might be attributable, at least in part, to its effect on susceptibility to MetS.
|
21784758 |
2011 |
|
rs6929846
|
|
|
0.780 |
GeneticVariation |
BEFREE |
We showed that the C→T polymorphism (rs6929846) of BTN2A1 and A→G polymorphism (rs2569512) of ILF3 were significantly associated with myocardial infarction in Japanese individuals by a genome-wide association study.
|
21557786 |
2011 |
|
rs6929846
|
|
|
0.780 |
GeneticVariation |
BEFREE |
Given that hypertension is a major risk factor for myocar</span>dial infarction, the association of rs6929846 of BTN2A1 with myocardial infarction</span> might be attributable, at least in part, to its effect on susceptibility to hypertension.
|
21525964 |
2011 |
|
rs6929846
|
|
|
0.780 |
GeneticVariation |
BEFREE |
The results suggest that the relationship between rs6929846 of BTN2A1 or rs2569512 of ILF3 and MI is influenced by the serum concentrations of HDL and LDL cholesterol, respectively.
|
21468600 |
2011 |