|
rs17465637
|
|
|
0.840 |
GeneticVariation |
BEFREE |
Genome-wide association studies have described an association between MIA3 rs17465637 A/C polymorphisms and coronary artery disease and myocardial infarction.
|
22577832 |
2012 |
|
rs17465637
|
|
|
0.840 |
GeneticVariation |
BEFREE |
SNPs were genotyped by TaqMan assays and follow-up multivariate logistic regression analysis with incorporation of significant covariates showed significant association with MI for MIA3 SNP rs17465637 (P-adj= 0.0034) and SORT1 SNP rs599839 (P-adj= 0.009).
|
21463265 |
2011 |
|
rs17465637
|
|
|
0.840 |
GeneticVariation |
BEFREE |
Showing association between rs17465637 and MI, this work was consistent with results from the original detection study and most prior replication studies addressing this issue.
|
21264445 |
2011 |
|
rs17465637
|
|
C |
0.840 |
GeneticVariation |
GWASCAT |
Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants.
|
19198609 |
2009 |
|
rs17465637
|
|
C |
0.840 |
GeneticVariation |
GWASDB |
Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants.
|
19198609 |
2009 |
|
rs17465637
|
|
|
0.840 |
GeneticVariation |
BEFREE |
Although the underlying mechanisms are not clearly understood, the previously reported association between the 2 SNPs (rs1333049 and rs17465637) and MI was reproduced in this Japanese sample.
|
18654002 |
2008 |
|
rs3782886
|
|
|
0.820 |
GeneticVariation |
BEFREE |
Since inflammation-related single-nucleotide polymorphism (SNP (rs3782886)) is reportedly associated with myocardial infarction and short stature, rs3782886 could be associated with a high platelet count and thus more intense endothelial repair activity.
|
31043174 |
2019 |
|
rs3782886
|
|
|
0.820 |
GeneticVariation |
BEFREE |
Asian-specific single nucleotide polymorphism (SNPs) (rs3782886) is reported to be associated with myocardial infarction; sarcopenia is reported to be associated with coronary subclinical atherosclerosis.
|
29165153 |
2017 |
|
rs9982601
|
|
|
0.820 |
GeneticVariation |
BEFREE |
Two other SNPs on the same gene, rs10757274_G [0.79(0.73-0.86); p = 2.98E-08] and rs1333045_C [0.79(0.73-0.86); p = 1.15E-08] as well as the rs9982601_T [1.38(1.23-1.55); p = 3.49E-08] on KCNE2 were associated with MI.
|
26708285 |
2016 |
|
rs9982601
|
|
T |
0.820 |
GeneticVariation |
GWASCAT |
Two other SNPs on the same gene, rs10757274_G [0.79(0.73-0.86); p = 2.98E-08] and rs1333045_C [0.79(0.73-0.86); p = 1.15E-08] as well as the rs9982601_T [1.38(1.23-1.55); p = 3.49E-08] on KCNE2 were associated with MI.
|
26708285 |
2016 |
|
rs12526453
|
|
|
0.820 |
GeneticVariation |
BEFREE |
The rs12526453 CC homozygotes (previously associated with increased risk of myocardial infarction) showed, in 2 independent samples, better long-term survival.
|
26086777 |
2015 |
|
rs3782886
|
|
A |
0.820 |
GeneticVariation |
GWASCAT |
A genome-wide association study identifies PLCL2 and AP3D1-DOT1L-SF3A2 as new susceptibility loci for myocardial infarction in Japanese.
|
24916648 |
2015 |
|
rs3782886
|
|
|
0.820 |
GeneticVariation |
GWASDB |
A genome-wide association study identifies PLCL2 and AP3D1-DOT1L-SF3A2 as new susceptibility loci for myocardial infarction in Japanese.
|
24916648 |
2015 |
|
rs9982601
|
|
|
0.820 |
GeneticVariation |
BEFREE |
We showed that the rs9982601 polymorphism of the region between SLC5A3/MRPS6 and KCNE2 genes is associated with long-term mortality in high-risk patients after MI.
|
25697262 |
2015 |
|
rs12526453
|
|
|
0.820 |
GeneticVariation |
BEFREE |
Besides the CAD/MI SNP at 9p21 (rs4977574, P = 3.1 × 10(-10)), two additional loci at ADAMTS7 (rs3825807, P = 6.5 × 10(-6)) and at PHACTR1 (rs12526453, P = 1.0 × 10(-3)) show a nominally significant association with coronary artery calcification with MI/CAD risk alleles increasing the degree of arterial calcification.
|
23561647 |
2013 |
|
rs3782886
|
|
|
0.820 |
GeneticVariation |
GWASDB |
SNPs on chromosome 5p15.3 associated with myocardial infarction in Japanese population.
|
21107343 |
2011 |
|
rs12526453
|
|
C |
0.820 |
GeneticVariation |
GWASCAT |
Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants.
|
19198609 |
2009 |
|
rs12526453
|
|
C |
0.820 |
GeneticVariation |
GWASDB |
Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants.
|
19198609 |
2009 |
|
rs9982601
|
|
T |
0.820 |
GeneticVariation |
GWASDB |
Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants.
|
19198609 |
2009 |
|
rs9982601
|
|
T |
0.820 |
GeneticVariation |
GWASCAT |
Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants.
|
19198609 |
2009 |
|
rs10738607
|
|
|
0.810 |
GeneticVariation |
BEFREE |
Four SNPs, rs4977574_A [0.56(0.50-0.63); p < 0.0001], rs10757274_A [0.87(0.77-0.97); p = 0.014], rs10738607_A [0.89(0.80-1.00); p = 0.043] and rs1333045_T [0.54(0.48-0.61); p < 0.0001] residing on the CDKN2B gene were significantly associated with CAD following multivariate adjustments for MI, HTN and DM, while four others were weakly associated with the disease.
|
29894795 |
2018 |
|
rs11206510
|
|
|
0.810 |
GeneticVariation |
BEFREE |
Two-sided <i>P</i> values <0.05 were considered significant.<b>Results:</b> We observed a significant interaction between the <i>PCSK9</i> rs11206510 genotype and LC n-3 PUFA intake on nonfatal MI risk (<i>P</i>-interaction = 0.012).
|
28330911 |
2017 |
|
rs10738607
|
|
G |
0.810 |
GeneticVariation |
GWASCAT |
A genome-wide association study reveals susceptibility loci for myocardial infarction/coronary artery disease in Saudi Arabs.
|
26708285 |
2016 |
|
rs11206510
|
|
T |
0.810 |
GeneticVariation |
GWASCAT |
A comprehensive 1,000 Genomes-based genome-wide association meta-analysis of coronary artery disease.
|
26343387 |
2015 |
|
rs1122608
|
|
|
0.810 |
GeneticVariation |
BEFREE |
We also found three SNPs rs1122608, rs3798220 and rs579459 were significantly associated with risk factors of MI, although they had no association with MI in Chinese population.
|
24475106 |
2014 |