Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs12035735
rs12035735
LRRC8D
0.700 GeneticVariation GWASCAT NUDT15 codon 139 is the best pharmacogenetic marker for predicting thiopurine-induced severe adverse events in Japanese patients with inflammatory bowel disease: a multicenter study. 29923122

2018
dbSNP: rs10419226
rs10419226
CRTC1
A 0.700 GeneticVariation GWASCAT A genome-wide association study identifies new susceptibility loci for esophageal adenocarcinoma and Barrett's esophagus. 24121790

2013
dbSNP: rs11789015
rs11789015
BARX1
A 0.700 GeneticVariation GWASCAT A genome-wide association study identifies new susceptibility loci for esophageal adenocarcinoma and Barrett's esophagus. 24121790

2013
dbSNP: rs2178146
rs2178146 		A 0.700 GeneticVariation GWASCAT A genome-wide association study identifies new susceptibility loci for esophageal adenocarcinoma and Barrett's esophagus. 24121790

2013
dbSNP: rs2687201
rs2687201 		T 0.700 GeneticVariation GWASCAT A genome-wide association study identifies new susceptibility loci for esophageal adenocarcinoma and Barrett's esophagus. 24121790

2013
dbSNP: rs3784262
rs3784262
ALDH1A2
A 0.700 GeneticVariation GWASCAT A genome-wide association study identifies new susceptibility loci for esophageal adenocarcinoma and Barrett's esophagus. 24121790

2013
dbSNP: rs4800353
rs4800353 		T 0.700 GeneticVariation GWASCAT A genome-wide association study identifies new susceptibility loci for esophageal adenocarcinoma and Barrett's esophagus. 24121790

2013
dbSNP: rs7632500
rs7632500
LOC107986152
C 0.700 GeneticVariation GWASCAT A genome-wide association study identifies new susceptibility loci for esophageal adenocarcinoma and Barrett's esophagus. 24121790

2013
dbSNP: rs7229639
rs7229639
SMAD7
0.010 GeneticVariation BEFREE Genome-wide association studies (GWAS) have identified three loci at 18q21 (rs4939827, rs7240004, and rs7229639), which maps to SMAD7 loci, were associated with risk of diseases of the digestive system. 26989026

2016
dbSNP: rs7240004
rs7240004 		0.010 GeneticVariation BEFREE Genome-wide association studies (GWAS) have identified three loci at 18q21 (rs4939827, rs7240004, and rs7229639), which maps to SMAD7 loci, were associated with risk of diseases of the digestive system. 26989026

2016
dbSNP: rs11362
rs11362
DEFB1
0.010 GeneticVariation BEFREE Our meta-analysis provides evidence that DEFB1 genetic polymorphisms rs11362G>A, rs1800972C>G and rs1799946G>A are important contributing factors to the development of digestive diseases. 26232989

2015
dbSNP: rs1799946
rs1799946
DEFB1
0.010 GeneticVariation BEFREE Our meta-analysis provides evidence that DEFB1 genetic polymorphisms rs11362G>A, rs1800972C>G and rs1799946G>A are important contributing factors to the development of digestive diseases. 26232989

2015
dbSNP: rs1800972
rs1800972
DEFB1
0.010 GeneticVariation BEFREE Our meta-analysis provides evidence that DEFB1 genetic polymorphisms rs11362G>A, rs1800972C>G and rs1799946G>A are important contributing factors to the development of digestive diseases. 26232989

2015