|
rs1883832
|
|
|
0.010 |
GeneticVariation |
BEFREE |
<b>Conclusions:</b> Our work showed a significant association between the -1 C>T (rs1883832) polymorphism of the CD40 gene and MI in the Tunisians.
|
30924686 |
2019 |
|
rs498005
|
|
|
0.010 |
GeneticVariation |
BEFREE |
<b>Results:</b> C allele of rs498005 was significantly correlated with increased risk of AF (OR = 1.412, 95%CI = 1.012-1.970), and the association still exited after adjustment by age, gender, the status of smoking and drinking, histories of diabetes, hyperlipidaemia and myocardial infarction (adjusted OR = 1.473, 95%CI = 1.043-2.081).
|
31315459 |
2019 |
|
rs1217691063
|
|
|
0.100 |
GeneticVariation |
BEFREE |
Myocardial infarction in a newborn heterozygous for the MTHFR C677T mutation.
|
22339112 |
2012 |
|
rs5443
|
|
|
0.070 |
GeneticVariation |
BEFREE |
C825T polymorphism in the G protein beta3 subunit gene (GNB3) has been associated with arterial hypertension, coronary artery disease and myocardial infarction.
|
10704626 |
2000 |
|
rs699
|
|
|
0.100 |
GeneticVariation |
BEFREE |
M235T genotype did not predict systolic or diastolic blood pressure or risk of ischemic heart disease or myocardial infarction in either ethnic group.
|
12805070 |
2003 |
|
rs1799983
|
|
|
0.100 |
GeneticVariation |
BEFREE |
G894T polymorphism on the eNOS gene increases the risk for premature MI and modifies the response of vascular endothelium during the acute phase of MI by affecting the release of vWF, IL-6, and oxidative stress status, an effect diminished one year after the event.
|
16168297 |
2005 |
|
rs3135507
|
|
|
0.010 |
GeneticVariation |
BEFREE |
Val153>Met variation in the APOAV gene plays a sex-specific role in genetic determination of plasma high-density lipoprotein cholesterol levels, but does not influence risk of MI in males.
|
16311097 |
2005 |
|
rs11666735
|
|
|
0.010 |
GeneticVariation |
BEFREE |
Asp92Asn polymorphism in the myeloid IgA Fc receptor is associated with myocardial infarction in two disparate populations: CARE and WOSCOPS.
|
17008591 |
2006 |
|
rs370102050
|
|
|
0.010 |
GeneticVariation |
BEFREE |
Asp92Asn polymorphism in the myeloid IgA Fc receptor is associated with myocardial infarction in two disparate populations: CARE and WOSCOPS.
|
17008591 |
2006 |
|
rs1057335
|
|
|
0.010 |
GeneticVariation |
BEFREE |
Arg407Lys was not associated with α2AP C-terminal cleavage, total α2AP antigen levels, or MI risk (odds ratios compared with Arg/Arg: Arg/Lys 0.74, 95% CI: 0.50-1.10; Lys/Lys 0.77, 95% CI: 0.31-1.92).
|
21505192 |
2011 |
|
rs4986970
|
|
|
0.010 |
GeneticVariation |
BEFREE |
The causal odds ratio for MI for a 50% reduction in plasma HDL cholesterol due to S208T genotype in both studies combined was 0.49 (0.11-2.16), whereas the hazard ratio for MI for a 50% reduction in plasma HDL cholesterol in the CCHS was 2.11 (1.70-2.62) (P(comparison) = 0.03).
|
22090275 |
2012 |
|
rs2943634
|
|
|
0.030 |
GeneticVariation |
BEFREE |
rs2943634 minor allele (A) was associated in an additive fashion with lower risk of IS but not with MI [hazard ratio (HR)=0.66; 95% confidence interval (CI): 0.50-0.87; P=0.003; HR=1.02; 95% CI: 0.82-1.28; P=0.83 respectively, for the age and sex adjusted model].
|
22207032 |
2012 |
|
rs4704397
|
|
|
0.010 |
GeneticVariation |
BEFREE |
rs4704397 is associated with thyroid function, risk of MI, and body height.
|
23941514 |
2014 |
|
rs671
|
|
|
0.040 |
GeneticVariation |
BEFREE |
A Glu487Lys polymorphism in the gene for mitochondrial aldehyde dehydrogenase 2 is associated with myocardial infarction in elderly Korean men.
|
17459359 |
2007 |
|
rs774229224
|
|
|
0.010 |
GeneticVariation |
BEFREE |
A common G-to-T point mutation (Val 34 Leu) in exon 2 of the alpha-subunit of the factor XIII is strongly negatively associated with the development of myocardial infarction.
|
9550516 |
1998 |
|
rs1333049
|
|
|
0.100 |
GeneticVariation |
BEFREE |
A common variant at chromosome 9p21 (tagged by the rs1333049 or rs10757278 single-nucleotide polymorphism) is strongly associated with myocardial infarction and major arterial aneurysms.
|
20031606 |
2009 |
|
rs10757278
|
|
|
0.900 |
GeneticVariation |
BEFREE |
A common variant at chromosome 9p21 (tagged by the rs1333049 or rs10757278 single-nucleotide polymorphism) is strongly associated with myocardial infarction and major arterial aneurysms.
|
20031606 |
2009 |
|
rs10757278
|
|
G |
0.900 |
GeneticVariation |
GWASCAT |
A common variant on chromosome 9p21 affects the risk of myocardial infarction.
|
17478679 |
2007 |
|
rs10757278
|
|
G |
0.900 |
GeneticVariation |
GWASDB |
A common variant on chromosome 9p21 affects the risk of myocardial infarction.
|
17478679 |
2007 |
|
rs4977574
|
|
|
0.880 |
GeneticVariation |
GWASDB |
A common variant on chromosome 9p21 affects the risk of myocardial infarction.
|
17478679 |
2007 |
|
rs10738607
|
|
|
0.810 |
GeneticVariation |
GWASDB |
A common variant on chromosome 9p21 affects the risk of myocardial infarction.
|
17478679 |
2007 |
|
rs2383207
|
|
|
0.770 |
GeneticVariation |
GWASDB |
A common variant on chromosome 9p21 affects the risk of myocardial infarction.
|
17478679 |
2007 |
|
rs1333045
|
|
|
0.730 |
GeneticVariation |
GWASDB |
A common variant on chromosome 9p21 affects the risk of myocardial infarction.
|
17478679 |
2007 |
|
rs1333040
|
|
|
0.720 |
GeneticVariation |
GWASDB |
A common variant on chromosome 9p21 affects the risk of myocardial infarction.
|
17478679 |
2007 |
|
rs10116277
|
|
|
0.700 |
GeneticVariation |
GWASDB |
A common variant on chromosome 9p21 affects the risk of myocardial infarction.
|
17478679 |
2007 |