|
rs397507444
|
|
|
0.090 |
GeneticVariation |
BEFREE |
The risk observed for A1298C was 2.28 and 2.12 times higher in variants (AC + CC) of both DVT and CAD (OR = 2.28, 95%CI = 1.09-4.75 and OR = 2.12, 95%CI = 1.02-4.40, respectively).
|
31571711 |
2020 |
|
rs397507444
|
|
|
0.090 |
GeneticVariation |
BEFREE |
Thus, the aim of the present study is to determine the prevalence of FVL, MTHFR C677T and MTHFR A1298C gene polymorphisms in patients with DVT in central Iran.
|
29855758 |
2018 |
|
rs397507444
|
|
|
0.090 |
GeneticVariation |
BEFREE |
The presence of homozygous MTHFR A1298C mutation was significantly associated with DVT (P=0.020).
|
21080081 |
2011 |
|
rs397507444
|
|
|
0.090 |
GeneticVariation |
BEFREE |
Factor V (FV)-Leiden (G16891A)-, factor II(G20210A)-mutations, protein C- and S, as well as methylenetetrahydrofolate reductase (MTHFR) polymorphisms at C677T and A1298C, and serum homocysteine levels (hcy) were determined in 29 patients with SVT and 26 with DVT.
|
20881312 |
2011 |
|
rs397507444
|
|
|
0.090 |
GeneticVariation |
BEFREE |
Recurrent deep vein thrombosis and pulmonary embolism in a young man with Klinefelter's syndrome and heterozygous mutation of MTHFR-677C>T and 1298A>C.
|
20449891 |
2010 |
|
rs397507444
|
|
|
0.090 |
GeneticVariation |
BEFREE |
We therefore compared the prevalence of factor V Leiden, prothrombin G20210A, methylenetetrahydrofolate reductase (MTHFR) C677T and A1298C, and plasminogen activator inhibitor 4G/5G polymorphisms between 50 patients with symptomatic DVT within 3 weeks after elective THA and an asymptomatic control group of 85 patients.
|
18800213 |
2009 |
|
rs397507444
|
|
|
0.090 |
GeneticVariation |
BEFREE |
Plasma concentration of tHcy in AC genotype of MTHFR A1298C was increased in patients with OAD and in patients with DVT.
|
18800176 |
2008 |
|
rs397507444
|
|
|
0.090 |
GeneticVariation |
BEFREE |
The prevalences of the C677T and A1298C genotypes did not differ significantly in 772 individuals with documented coronary artery disease (CAD), 137 individuals with deep-vein thrombosis (DVT), and 329 individuals without documented vascular disease.
|
11274015 |
2001 |
|
rs397507444
|
|
|
0.090 |
GeneticVariation |
BEFREE |
These data do not support a critical role of MTHFR 1298 A --> C in the predisposition to DVT.
|
10233437 |
1999 |