rs1057519328
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs146597836
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs746055479
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs750868279
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs751454741
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs752615209
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs755659290
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs774164456
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs886039866
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs886040969
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs751377893
|
|
|
0.030 |
GeneticVariation |
BEFREE |
We investigated the prevalence of the coagulation factor V gene G1691A mutation in 64 patients with Behçet's disease (BD) and in 107 apparently healthy individuals.
|
8948311 |
1996 |
rs3743930
|
|
|
0.050 |
GeneticVariation |
BEFREE |
The M694V, V726A and E148Q mutations tended to be more frequent in definite BD (2.6%, 2.6%, and 5.2%, respectively) than in controls (0%, 0%, and 2.2%).
|
10980540 |
2000 |
rs61752717
|
|
|
0.040 |
GeneticVariation |
BEFREE |
The M694V, V726A and E148Q mutations tended to be more frequent in definite BD (2.6%, 2.6%, and 5.2%, respectively) than in controls (0%, 0%, and 2.2%).
|
10980540 |
2000 |
rs28940579
|
|
|
0.020 |
GeneticVariation |
BEFREE |
The M694V, V726A and E148Q mutations tended to be more frequent in definite BD (2.6%, 2.6%, and 5.2%, respectively) than in controls (0%, 0%, and 2.2%).
|
10980540 |
2000 |
rs1217691063
|
|
|
0.090 |
GeneticVariation |
BEFREE |
MTHFR gene C677T mutation does not increase risk of DVT in BD either alone or combined with FV Leiden mutation.
|
11128675 |
2000 |
rs1188383936
|
|
|
0.030 |
GeneticVariation |
BEFREE |
MTHFR gene C677T mutation does not increase risk of DVT in BD either alone or combined with FV Leiden mutation.
|
11128675 |
2000 |
rs899127658
|
|
|
0.030 |
GeneticVariation |
BEFREE |
Possible roles of methylenetetrahydrofolate reductase (MTHFR) gene C677T, factor V (FV) gene G1691A (Leiden), and prothrombin gene G20210A polymorphisms in venous thrombogenesis were evaluated in patients with BD; 100 healthy people, 30 BD patients without DVT, 30 BD patients with DVT, and 30 patients with idiopathic DVT were studied with the restriction fragment length polymorphism method for these 3 polymorphisms.
|
11128675 |
2000 |
rs1799969
|
|
|
0.030 |
GeneticVariation |
BEFREE |
Our findings show that G/R 241 polymorphism of ICAM-1 is associated with BD susceptibility.
|
11409120 |
2001 |
rs1061622
|
|
|
0.010 |
GeneticVariation |
BEFREE |
In this study, we investigated genetic polymorphisms of TNF alpha -308 G/A, TNF beta +252 G/A, and TNFR2 196 R/M in 94 Korean BD patients and age- and sex-matched healthy controls to investigate the role of TNF and TNF receptor polymorphisms in BD.
|
12770792 |
2003 |
rs1217691063
|
|
|
0.090 |
GeneticVariation |
BEFREE |
The rates of homozygosity for the MTHFR C677T mutation in the BD and HC groups were 7.5% and 10%, respectively.
|
14504916 |
2003 |
rs1799983
|
|
|
0.070 |
GeneticVariation |
BEFREE |
The Glu298Asp polymorphism in exon 7 of the eNOS gene seems to be a susceptibility gene for Korean BD and other rheumatic diseases.
|
14583572 |
2003 |
rs28940579
|
|
|
0.020 |
GeneticVariation |
BEFREE |
The frequencies of three FMF-related MEFV mutations (M694V, M680I and V726A) were investigated in BD patients (n = 57) by molecular genetic studies using a polymerase chain reaction with the ARMS method.
|
14727457 |
2004 |
rs751377893
|
|
|
0.030 |
GeneticVariation |
BEFREE |
To evaluate the frequency and type of vascular lesions and to study the association of factor V gene G1691A (Leiden) and prothrombin gene G20210A polymorphisms with venous thrombosis in Italian patients with Behçet's disease (BD).
|
15077257 |
2004 |
rs899127658
|
|
|
0.030 |
GeneticVariation |
BEFREE |
To evaluate the frequency and type of vascular lesions and to study the association of factor V gene G1691A (Leiden) and prothrombin gene G20210A polymorphisms with venous thrombosis in Italian patients with Behçet's disease (BD).
|
15077257 |
2004 |
rs2010963
|
|
|
0.010 |
GeneticVariation |
BEFREE |
All patients with BD and controls were genotyped by polymerase chain reaction and allele-specific oligonucleotide techniques for +936 C/T (rs3025039) and -634 C/G (rs2010963) mutations and for an 18 base pair (bp) insertion/deletion (I/D) polymorphism at -2549 of the the VEGF promoter region.
|
15338501 |
2004 |