Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs4240384
rs4240384
0.700 GeneticVariation GWASCAT Genetic variants at the 16p13 locus confer risk for eosinophilic esophagitis. 29904099

2019

dbSNP: rs8008716
rs8008716
G 0.700 GeneticVariation GWASCAT GWAS identifies four novel eosinophilic esophagitis loci. 25407941

2014

dbSNP: rs371915
rs371915
0.700 GeneticVariation GWASCAT Common variants at 5q22 associate with pediatric eosinophilic esophagitis. 20208534

2010

dbSNP: rs1059513
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

dbSNP: rs2075277
rs2075277
0.700 GeneticVariation GWASCAT Genome-wide association analysis of eosinophilic esophagitis provides insight into the tissue specificity of this allergic disease. 25017104

2014

dbSNP: rs11206830
rs11206830
0.700 GeneticVariation GWASCAT Genome-wide association analysis of eosinophilic esophagitis provides insight into the tissue specificity of this allergic disease. 25017104

2014

dbSNP: rs1986734
rs1986734
0.700 GeneticVariation GWASCAT Common variants at 5q22 associate with pediatric eosinophilic esophagitis. 20208534

2010

dbSNP: rs167769
rs167769
T 0.700 GeneticVariation GWASCAT GWAS identifies four novel eosinophilic esophagitis loci. 25407941

2014

dbSNP: rs324011
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

dbSNP: rs3744790
rs3744790
0.700 GeneticVariation GWASCAT Genome-wide association analysis of eosinophilic esophagitis provides insight into the tissue specificity of this allergic disease. 25017104

2014

dbSNP: rs3806932
rs3806932
0.720 GeneticVariation GWASCAT Common variants at 5q22 associate with pediatric eosinophilic esophagitis. 20208534

2010

dbSNP: rs3806932
rs3806932
0.720 GeneticVariation BEFREE We report association of EoE with variants at chromosome 5q22 encompassing TSLP and WDR36 (rs3806932, combined P = 3.19 x 10(-9)). 20208534

2010

dbSNP: rs3806932
rs3806932
0.720 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

dbSNP: rs3806933
rs3806933
G 0.700 GeneticVariation GWASCAT Genome-wide association analysis of eosinophilic esophagitis provides insight into the tissue specificity of this allergic disease. 25017104

2014

dbSNP: rs10062929
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

dbSNP: rs2416257
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

dbSNP: rs2898261
rs2898261
C 0.700 GeneticVariation GWASCAT Genome-wide association analysis of eosinophilic esophagitis provides insight into the tissue specificity of this allergic disease. 25017104

2014