|
rs1217691063
|
|
|
0.020 |
GeneticVariation |
BEFREE |
Association of methylenetetrahydrofolate reductase (MTHFR 677C>T and 1298A>C) polymorphisms and haplotypes with silent brain infarction and homocysteine levels in a Korean population.
|
20191019 |
2010 |
|
rs1217691063
|
|
|
0.020 |
GeneticVariation |
BEFREE |
However, the association of homozygous C677T MTHFR mutation with silent brain infarctions in infancy has not been reported.
|
16814086 |
2006 |
|
rs699
|
|
|
0.010 |
GeneticVariation |
BEFREE |
In East Asian group, significant association was found between AGT M235T polymorphism and risk of MI (for dominant model: OR=1.79; 95% CI=1.04-3.06; for recessive model OR=2.01; 95% CI=1.21-3.36; for additive model OR=1.79; 95% CI=1.14-2.86) as well as BI (for dominant model: OR=1.66; 95% CI=1.22-2.27; for recessive model OR=1.78, 95% CI=1.29-2.46; for additive model: OR=1.64, 95% CI=1.34-2.00), while the M235T polymorphism did not impact the risk of MI in total population and other ethnicity.
|
23933419 |
2013 |
|
rs397507444
|
|
|
0.010 |
GeneticVariation |
BEFREE |
Association of methylenetetrahydrofolate reductase (MTHFR 677C>T and 1298A>C) polymorphisms and haplotypes with silent brain infarction and homocysteine levels in a Korean population.
|
20191019 |
2010 |
|
rs1400106676
|
|
|
0.010 |
GeneticVariation |
BEFREE |
Comparison of allele frequencies between 1112 cases with brain infarction and age- and sex-matched control subjects of the same number found an SNP in the 5'-flanking region of angiotensin receptor like-1 (AGTRL1) gene (rs9943582, - 154G/A) to have a significant association with brain infarction [odds ratio = 1.30, 95% confidence interval (CI) = 1.14-1.47, P = 0.000066].
|
17309882 |
2007 |
|
rs532019808
|
|
|
0.010 |
GeneticVariation |
BEFREE |
Here, we investigate the relationship between the C242T polymorphism and brain infarction in Japan.
|
17880563 |
2007 |
|
rs9943582
|
|
|
0.010 |
GeneticVariation |
BEFREE |
Comparison of allele frequencies between 1112 cases with brain infarction and age- and sex-matched control subjects of the same number found an SNP in the 5'-flanking region of angiotensin receptor like-1 (AGTRL1) gene (rs9943582, - 154G/A) to have a significant association with brain infarction [odds ratio = 1.30, 95% confidence interval (CI) = 1.14-1.47, P = 0.000066].
|
17309882 |
2007 |
|
rs1799945
|
|
|
0.010 |
GeneticVariation |
BEFREE |
In the present work, we have determined the HFE genotypes for C282Y and H63D in subjects from two case-control studies: the ECTIM and GENIC studies, designed to identify genetic variants associated with myocardial and brain infarction, respectively.
|
11380589 |
2001 |
|
rs1800562
|
|
|
0.010 |
GeneticVariation |
BEFREE |
In the present work, we have determined the HFE genotypes for C282Y and H63D in subjects from two case-control studies: the ECTIM and GENIC studies, designed to identify genetic variants associated with myocardial and brain infarction, respectively.
|
11380589 |
2001 |
|
rs268
|
|
|
0.010 |
GeneticVariation |
BEFREE |
The Asn291Ser polymorphism was not significantly associated with brain infarction.
|
11680797 |
2001 |
|
rs45567233
|
|
|
0.010 |
GeneticVariation |
BEFREE |
We identified 4 polymorphisms in the 5'-flanking region (G-618C, G-315A, C-179T, and C-160T) and 1 polymorphism in the coding region (Asn125Ser) of the gene and genotyped the participants in the Etude Cas-Temoins sur l'Infarctus du Myocarde (ECTIM Study), a case-control study for MI, and in the Etude du Profil Génétique de l'Infarctus Cérébral (GENIC Study), a case-control study for brain infarction (BI), for all identified genetic variants.
|
11557685 |
2001 |
|
rs1799983
|
|
|
0.010 |
GeneticVariation |
BEFREE |
Homozygosity for the G allele of the Glu298Asp polymorphism in NOS3 was associated with BI, and especially with lacunar stroke.
|
10884465 |
2000 |