Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs11819199
rs11819199 		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: rs2000260
rs2000260 		A 0.700 GeneticVariation GWASCAT Genome-wide association analysis of eosinophilic esophagitis provides insight into the tissue specificity of this allergic disease. 25017104

2014
dbSNP: rs2055376
rs2055376 		A 0.700 GeneticVariation GWASCAT Genome-wide association analysis of eosinophilic esophagitis provides insight into the tissue specificity of this allergic disease. 25017104

2014
dbSNP: rs2155219
rs2155219 		A 0.700 GeneticVariation GWASCAT Genome-wide association analysis of eosinophilic esophagitis provides insight into the tissue specificity of this allergic disease. 25017104

2014
dbSNP: rs252716
rs252716 		C 0.700 GeneticVariation GWASCAT GWAS identifies four novel eosinophilic esophagitis loci. 25407941

2014
dbSNP: rs599707
rs599707 		0.700 GeneticVariation GWASCAT Genetic variants at the 16p13 locus confer risk for eosinophilic esophagitis. 29904099

2019
dbSNP: rs6799767
rs6799767 		0.700 GeneticVariation GWASCAT Common variants at 5q22 associate with pediatric eosinophilic esophagitis. 20208534

2010
dbSNP: rs8041227
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
dbSNP: rs3815700
rs3815700
ANKRD27
C 0.700 GeneticVariation GWASCAT GWAS identifies four novel eosinophilic esophagitis loci. 25407941

2014
dbSNP: rs4671393
rs4671393
BCL11A
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
dbSNP: rs489441
rs489441
C5orf66
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
dbSNP: rs149864795
rs149864795
CAPN14
A 0.700 GeneticVariation GWASCAT GWAS identifies four novel eosinophilic esophagitis loci. 25407941

2014
dbSNP: rs77569859
rs77569859
CAPN14
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: rs6736278
rs6736278
CAPN14
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
dbSNP: rs77301713
rs77301713
CAPN5
0.700 GeneticVariation GWASCAT Genome-wide association analysis of eosinophilic esophagitis provides insight into the tissue specificity of this allergic disease. 25017104

2014
dbSNP: rs118086209
rs118086209
CCDC81
C 0.700 GeneticVariation GWASCAT Genome-wide association analysis of eosinophilic esophagitis provides insight into the tissue specificity of this allergic disease. 25017104

2014
dbSNP: rs12924112
rs12924112
CLEC16A
0.700 GeneticVariation GWASCAT Genetic variants at the 16p13 locus confer risk for eosinophilic esophagitis. 29904099

2019
dbSNP: rs9956738
rs9956738
DCC
0.700 GeneticVariation GWASCAT Genome-wide association analysis of eosinophilic esophagitis provides insight into the tissue specificity of this allergic disease. 25017104

2014
dbSNP: rs61894547
rs61894547
EMSY
T 0.700 GeneticVariation GWASCAT GWAS identifies four novel eosinophilic esophagitis loci. 25407941

2014
dbSNP: rs7482144
rs7482144
HBG2
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
dbSNP: rs9399137
rs9399137
HBS1L
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
dbSNP: rs17004598
rs17004598
HSF2BP ; RRP1B
C 0.700 GeneticVariation GWASCAT Genome-wide association analysis of eosinophilic esophagitis provides insight into the tissue specificity of this allergic disease. 25017104

2014
dbSNP: rs28530674
rs28530674
IFFO2
0.700 GeneticVariation GWASCAT Genome-wide association analysis of eosinophilic esophagitis provides insight into the tissue specificity of this allergic disease. 25017104

2014
dbSNP: rs11495981
rs11495981
JAZF1
0.700 GeneticVariation GWASCAT Genetic variants at the 16p13 locus confer risk for eosinophilic esophagitis. 29904099

2019
dbSNP: rs2296225
rs2296225
KIF17
0.700 GeneticVariation GWASCAT Genome-wide association analysis of eosinophilic esophagitis provides insight into the tissue specificity of this allergic disease. 25017104

2014