|
rs10757278
|
|
Myocardial Infarction
|
G |
0.900 |
GeneticVariation
|
GWASDB |
A common variant on chromosome 9p21 affects the risk of myocardial infarction.
|
17478679 |
2007 |
|
rs10757278
|
|
Myocardial Infarction
|
G |
0.900 |
GeneticVariation
|
GWASCAT |
A common variant on chromosome 9p21 affects the risk of myocardial infarction.
|
17478679 |
2007 |
|
rs4977574
|
|
Myocardial Infarction
|
G |
0.880 |
GeneticVariation
|
GWASDB |
Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants.
|
19198609 |
2009 |
|
rs4977574
|
|
Myocardial Infarction
|
G |
0.880 |
GeneticVariation
|
GWASCAT |
Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants.
|
19198609 |
2009 |
|
rs4977574
|
|
Myocardial Infarction
|
|
0.880 |
GeneticVariation
|
GWASDB |
A common variant on chromosome 9p21 affects the risk of myocardial infarction.
|
17478679 |
2007 |
|
rs17465637
|
|
Myocardial Infarction
|
C |
0.840 |
GeneticVariation
|
GWASDB |
Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants.
|
19198609 |
2009 |
|
rs17465637
|
|
Myocardial Infarction
|
C |
0.840 |
GeneticVariation
|
GWASCAT |
Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants.
|
19198609 |
2009 |
|
rs12526453
|
|
Myocardial Infarction
|
C |
0.820 |
GeneticVariation
|
GWASCAT |
Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants.
|
19198609 |
2009 |
|
rs12526453
|
|
Myocardial Infarction
|
C |
0.820 |
GeneticVariation
|
GWASDB |
Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants.
|
19198609 |
2009 |
|
rs3782886
|
|
Myocardial Infarction
|
|
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 |
|
rs3782886
|
|
Myocardial Infarction
|
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
|
|
Myocardial Infarction
|
|
0.820 |
GeneticVariation
|
GWASDB |
SNPs on chromosome 5p15.3 associated with myocardial infarction in Japanese population.
|
21107343 |
2011 |
|
rs9982601
|
|
Myocardial Infarction
|
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 |
|
rs9982601
|
|
Myocardial Infarction
|
T |
0.820 |
GeneticVariation
|
GWASCAT |
Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants.
|
19198609 |
2009 |
|
rs9982601
|
|
Myocardial Infarction
|
T |
0.820 |
GeneticVariation
|
GWASDB |
Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants.
|
19198609 |
2009 |
|
rs10738607
|
|
Myocardial Infarction
|
G |
0.810 |
GeneticVariation
|
GWASCAT |
A genome-wide association study reveals susceptibility loci for myocardial infarction/coronary artery disease in Saudi Arabs.
|
26708285 |
2016 |
|
rs10738607
|
|
Myocardial Infarction
|
|
0.810 |
GeneticVariation
|
GWASDB |
A common variant on chromosome 9p21 affects the risk of myocardial infarction.
|
17478679 |
2007 |
|
rs11206510
|
|
Myocardial Infarction
|
T |
0.810 |
GeneticVariation
|
GWASCAT |
A comprehensive 1,000 Genomes-based genome-wide association meta-analysis of coronary artery disease.
|
26343387 |
2015 |
|
rs11206510
|
|
Myocardial Infarction
|
T |
0.810 |
GeneticVariation
|
GWASDB |
Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants.
|
19198609 |
2009 |
|
rs11206510
|
|
Myocardial Infarction
|
T |
0.810 |
GeneticVariation
|
GWASCAT |
Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants.
|
19198609 |
2009 |
|
rs1122608
|
|
Myocardial Infarction
|
G |
0.810 |
GeneticVariation
|
GWASCAT |
Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants.
|
19198609 |
2009 |
|
rs1122608
|
|
Myocardial Infarction
|
G |
0.810 |
GeneticVariation
|
GWASDB |
Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants.
|
19198609 |
2009 |
|
rs646776
|
|
Myocardial Infarction
|
T |
0.810 |
GeneticVariation
|
GWASCAT |
Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants.
|
19198609 |
2009 |
|
rs646776
|
|
Myocardial Infarction
|
T |
0.810 |
GeneticVariation
|
GWASDB |
Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants.
|
19198609 |
2009 |
|
rs11748327
|
|
Myocardial Infarction
|
|
0.800 |
GeneticVariation
|
GWASDB |
SNPs on chromosome 5p15.3 associated with myocardial infarction in Japanese population.
|
21107343 |
2011 |