|
rs77301713
|
|
|
0.700 |
GeneticVariation |
GWASCAT |
Genome-wide association analysis of eosinophilic esophagitis provides insight into the tissue specificity of this allergic disease.
|
25017104 |
2014 |
|
rs77569859
|
|
G |
0.700 |
GeneticVariation |
GWASCAT |
Genome-wide association analysis of eosinophilic esophagitis provides insight into the tissue specificity of this allergic disease.
|
25017104 |
2014 |
|
rs8008716
|
|
G |
0.700 |
GeneticVariation |
GWASCAT |
GWAS identifies four novel eosinophilic esophagitis loci.
|
25407941 |
2014 |
|
rs8041227
|
|
G |
0.700 |
GeneticVariation |
GWASCAT |
Genome-wide association analysis of eosinophilic esophagitis provides insight into the tissue specificity of this allergic disease.
|
25017104 |
2014 |
|
rs9956738
|
|
|
0.700 |
GeneticVariation |
GWASCAT |
Genome-wide association analysis of eosinophilic esophagitis provides insight into the tissue specificity of this allergic disease.
|
25017104 |
2014 |
|
rs1986734
|
|
|
0.700 |
GeneticVariation |
GWASCAT |
Common variants at 5q22 associate with pediatric eosinophilic esophagitis.
|
20208534 |
2010 |
|
rs371915
|
|
|
0.700 |
GeneticVariation |
GWASCAT |
Common variants at 5q22 associate with pediatric eosinophilic esophagitis.
|
20208534 |
2010 |
|
rs6799767
|
|
|
0.700 |
GeneticVariation |
GWASCAT |
Common variants at 5q22 associate with pediatric eosinophilic esophagitis.
|
20208534 |
2010 |
|
rs1059513
|
|
|
0.010 |
GeneticVariation |
BEFREE |
Carriage of STAT6 allelic variant rs1059513 predicts PPI-REE (OR [95% CI] = 6.16 [1.44, 26.4], P = 0.028), whereas carriage of STAT6 rs324011 synergizes with CYP2C1917 to predict PPI-nonresponsive EoE (rs324011 OR [95% CI] = 5.56 [1.33, 20.72], P = 0.022; CYP2C1917 OR [95% CI] = 8.19[1.42, 50.57], P = 0.023).
|
31490856 |
2019 |
|
rs324011
|
|
|
0.010 |
GeneticVariation |
BEFREE |
Carriage of STAT6 allelic variant rs1059513 predicts PPI-REE (OR [95% CI] = 6.16 [1.44, 26.4], P = 0.028), whereas carriage of STAT6 rs324011 synergizes with CYP2C1917 to predict PPI-nonresponsive EoE (rs324011 OR [95% CI] = 5.56 [1.33, 20.72], P = 0.022; CYP2C1917 OR [95% CI] = 8.19[1.42, 50.57], P = 0.023).
|
31490856 |
2019 |
|
rs6736278
|
|
|
0.010 |
GeneticVariation |
BEFREE |
In particular, breast-feeding in those with the susceptibility gene variant at rs6736278 (CAPN14) reduced the risk of EoE (adjusted odds ratio, 0.08; 95% CI, 0.01-0.59).
|
29029802 |
2018 |
|
rs2416257
|
|
|
0.010 |
GeneticVariation |
BEFREE |
For TSLP-WDR36 region, rs3806932 (G allele protective against eosinophilic esophagitis) and rs2416257 (A allele associated with lower eosinophil counts and protective against asthma) were correlated with decreased expression of TSLP in BAL (P = 7.9 × 10(-11) and 5.4 × 10(-4) , respectively) and BEC, but not WDR36.
|
26119467 |
2015 |
|
rs4671393
|
|
|
0.010 |
GeneticVariation |
BEFREE |
The result demonstrated that multiple genetic modifying factors including T allele of (G)γ-XmnI polymorphism (rs7482144), G allele of HBS1L-MYB (rs489441), C allele of HBS1L-MYB (rs9399137) and C allele of BCL11A (rs4671393) are associated with increased Hb F and in combination could explain approximately 80% of the variation of Hb F in Hb EE disease in Thai population.
|
24581976 |
2015 |
|
rs489441
|
|
|
0.010 |
GeneticVariation |
BEFREE |
The result demonstrated that multiple genetic modifying factors including T allele of (G)γ-XmnI polymorphism (rs7482144), G allele of HBS1L-MYB (rs489441), C allele of HBS1L-MYB (rs9399137) and C allele of BCL11A (rs4671393) are associated with increased Hb F and in combination could explain approximately 80% of the variation of Hb F in Hb EE disease in Thai population.
|
24581976 |
2015 |
|
rs7482144
|
|
|
0.010 |
GeneticVariation |
BEFREE |
The result demonstrated that multiple genetic modifying factors including T allele of (G)γ-XmnI polymorphism (rs7482144), G allele of HBS1L-MYB (rs489441), C allele of HBS1L-MYB (rs9399137) and C allele of BCL11A (rs4671393) are associated with increased Hb F and in combination could explain approximately 80% of the variation of Hb F in Hb EE disease in Thai population.
|
24581976 |
2015 |
|
rs9399137
|
|
|
0.010 |
GeneticVariation |
BEFREE |
The result demonstrated that multiple genetic modifying factors including T allele of (G)γ-XmnI polymorphism (rs7482144), G allele of HBS1L-MYB (rs489441), C allele of HBS1L-MYB (rs9399137) and C allele of BCL11A (rs4671393) are associated with increased Hb F and in combination could explain approximately 80% of the variation of Hb F in Hb EE disease in Thai population.
|
24581976 |
2015 |
|
rs10062929
|
|
|
0.010 |
GeneticVariation |
BEFREE |
A single SNP residing in the TSLP gene reached Bonferroni linkage disequilibrium-adjusted significance but only when patients with EE were compared with allergic control subjects (rs10062929; P = 4.11 x 10(-5); odds ratio, 0.35).
|
20620568 |
2010 |