|
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 |
|
|
|
|
rs1799969
|
|
|
0.030 |
GeneticVariation |
BEFREE |
Behçet's disease was associated with the ICAM1 E469, genotype ICAM1 469 E/E, ICAM1 241 G/R polymorphisms in different ethnic groups.
|
24645721 |
2014 |
|
rs1799983
|
|
|
0.070 |
GeneticVariation |
BEFREE |
Glu298 --> Asp polymorphism of the eNOS gene does not appear to be associated with the presence of BD in the Turkish population.
|
16463158 |
2006 |
|
rs7028891
|
|
|
0.010 |
GeneticVariation |
BEFREE |
A decreased frequency of the A allele of <i>TNFSF8</i>/rs7028891 was observed in BD patients.
|
29285231 |
2017 |
|
rs10454134
|
|
|
0.010 |
GeneticVariation |
BEFREE |
A higher frequency of both the rs10454134 AG genotypes (p = 0.008, OR = 1.413, 95% CI = 1.094-1.826) and a lower GG genotype frequency (p = 0.003, OR = 0.630, 95% CI = 0.465-0.854) were found in BD patients compared to the controls in the first stage.
|
31223615 |
2019 |
|
rs1805110
|
|
|
0.020 |
GeneticVariation |
BEFREE |
A polymorphism in TGFBR3 (rs1805110) has previously been identified in Han Chinese patients with BD.
|
25677673 |
2015 |
|
rs12785878
|
|
|
0.010 |
GeneticVariation |
BEFREE |
A second stage and combined study confirmed the association of r</span>s12785878 DHCR7 TT genotype and T allele with ocular Behçet disease (P = 3.28E-04 with Bonferroni correction; odds ratio, 1.506; 95% confidence interval, 1.248 to 1.818; and P = 2.82E-05 with Bonferroni correction; odds ratio, 1.339; 95% confidence interval, 1.188 to 1.508, respectively).
|
24184224 |
2014 |
|
rs11230563
|
|
|
0.010 |
GeneticVariation |
BEFREE |
A significantly higher frequency of the CT genotype, and a lower frequency of the CC genotype and C allele of CD6 rs11230563 were observed in BD as compared with controls.
|
27108704 |
2016 |
|
rs2293152
|
|
|
0.020 |
GeneticVariation |
BEFREE |
A significantly increased frequency of the GG genotype of the STAT3 rs2293152 was observed in patients with BD (Bonferroni-corrected P value = 0.021).
|
22205606 |
2012 |
|
rs3811047
|
|
|
0.010 |
GeneticVariation |
BEFREE |
A significantly lower frequency of the AG genotype, and a higher frequency of the GG genotype and G allele of IL-37/rs3811047 were observed in BD as compared to controls.
|
27775096 |
2016 |
|
rs11614913
|
|
|
0.010 |
GeneticVariation |
BEFREE |
A stratified analysis showed an association of the rs11614913 TT genotype and T allele with the arthritis subgroup of BD (P(c) = 5.3 × 10(-3), OR = 1.89; P(c) = 0.015, OR = 1.56, respectively).
|
23928854 |
2013 |
|
rs4986790
|
|
|
0.010 |
GeneticVariation |
BEFREE |
A total of 189 Italian patients who satisfied the International Study Group criteria for BD and 210 healthy age- and sex-matched blood donors were genotyped for two coding single nucleotide polymorphisms of TLR4 (Asp299Gly and Thr399Ile) by molecular methods.
|
19796532 |
2010 |
|
rs4986791
|
|
|
0.010 |
GeneticVariation |
BEFREE |
A total of 189 Italian patients who satisfied the International Study Group criteria for BD and 210 healthy age- and sex-matched blood donors were genotyped for two coding single nucleotide polymorphisms of TLR4 (Asp299Gly and Thr399Ile) by molecular methods.
|
19796532 |
2010 |
|
rs2058660
|
|
|
0.010 |
GeneticVariation |
BEFREE |
AA genotype and A allele frequency of IL-18RAP/rs2058660 was significantly decreased in BD as compared to controls.
|
27775096 |
2016 |
|
rs3743930
|
|
|
0.050 |
GeneticVariation |
BEFREE |
All BD patients were genotyped using polymerase chain reaction (PCR) and restriction enzyme analysis for the three most common MEFV mutations (M694V, V726A, and E148Q).
|
17454935 |
2007 |
|
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 |