|
rs1217691063
|
|
|
0.040 |
GeneticVariation |
BEFREE |
Polymorphism in the methylenetetrahydrofolate reductase (C677T) gene and homocysteine levels: a comparison in Brazilian patients with coronary arterial disease, ischemic stroke and peripheral arterial obstructive disease.
|
18040753 |
2009 |
|
rs1217691063
|
|
|
0.040 |
GeneticVariation |
BEFREE |
To clarify the contribution of C677T MTHFR mutation in arterial occlusive disease (AOD) or venous thromboembolism (VTE), we performed a case-controlled study including 160 cases with AOD and 180 cases with VTE attending our referral center and compared them with 200 matched healthy controls.
|
10477457 |
1999 |
|
rs1217691063
|
|
|
0.040 |
GeneticVariation |
BEFREE |
Factor V Leiden (a point mutation [1691G-->A] in the factor V gene), the prothrombin 20210G-->A mutation, and homozygosity for a common polymorphism in the methylene tetrahydrofolate reductase (MTHFR) gene (677C-->T) have been associated with arterial and venous thrombosis and arterial occlusive disease.
|
10360908 |
1999 |
|
rs1217691063
|
|
|
0.040 |
GeneticVariation |
BEFREE |
A common C677T mutation in the gene for the enzyme 5,10-methylenetetrahydrofolate reductase (5,10-MTHFR) has been linked to elevated levels of homocysteine and was therefore suspected to be a candidate genetic risk factor for arterial occlusive disease.
|
9950259 |
1999 |
|
rs1188383936
|
|
|
0.010 |
GeneticVariation |
BEFREE |
Factor V Leiden (a point mutation [1691G-->A] in the factor V gene), the prothrombin 20210G-->A mutation, and homozygosity for a common polymorphism in the methylene tetrahydrofolate reductase (MTHFR) gene (677C-->T) have been associated with arterial and venous thrombosis and arterial occlusive disease.
|
10360908 |
1999 |
|
rs751377893
|
|
|
0.010 |
GeneticVariation |
BEFREE |
Factor V Leiden (a point mutation [1691G-->A] in the factor V gene), the prothrombin 20210G-->A mutation, and homozygosity for a common polymorphism in the methylene tetrahydrofolate reductase (MTHFR) gene (677C-->T) have been associated with arterial and venous thrombosis and arterial occlusive disease.
|
10360908 |
1999 |
|
rs899127658
|
|
|
0.010 |
GeneticVariation |
BEFREE |
Factor V Leiden (a point mutation [1691G-->A] in the factor V gene), the prothrombin 20210G-->A mutation, and homozygosity for a common polymorphism in the methylene tetrahydrofolate reductase (MTHFR) gene (677C-->T) have been associated with arterial and venous thrombosis and arterial occlusive disease.
|
10360908 |
1999 |