Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs3738894
rs3738894
0.010 GeneticVariation BEFREE The gene-Environment interaction between rs3738894 and smoking history was associated with the risk of esophageal cancer. 31269493

2020

dbSNP: rs1048943
rs1048943
0.010 GeneticVariation BEFREE In additional, five variants on five genes were rated as strong cumulative epidemiological evidence for a nominally significant association with EC and ESCC risk, including CYP1A1 rs1048943, EGF rs444903, HOTAIR rs920778, MMP2 rs243865, and PLCE1 rs2274223, 10 variants were rated as moderate, and 18 variants were rated as weak. 30793520

2019

dbSNP: rs10509670
rs10509670
0.010 GeneticVariation BEFREE Results showed that the minor alleles of rs3765524, rs2274223, and rs10509670 were associated with increased risk of EC and GC. 30931333

2019

dbSNP: rs115510139
rs115510139
0.010 GeneticVariation BEFREE Stratified analysis was performed by gender, age, alcohol drinking, BMI, TNM stage and lymph node metastasis, the results showed that rs7436, rs115510139 and rs6720283 were significantly associated with the risk of EC in different groups (all p < 0.05). 31425922

2019

dbSNP: rs11674595
rs11674595
0.010 GeneticVariation BEFREE Our results reveal the significant association between SNPs (rs11674595 and rs2072472) in the IL1R2 and EC risk in the Chinese Han population. 31744444

2019

dbSNP: rs2031920
rs2031920
0.010 GeneticVariation BEFREE The <i>CYP1A1</i> rs4646903 and <i>CYP2E1</i> rs2031920 polymorphisms were risk factors of GCC or EC, and the <i>GSTM1</i> null genotype may serve a protective role against EC. 31423187

2019

dbSNP: rs2072472
rs2072472
0.010 GeneticVariation BEFREE Our results reveal the significant association between SNPs (rs11674595 and rs2072472) in the IL1R2 and EC risk in the Chinese Han population. 31744444

2019

dbSNP: rs2094258
rs2094258
0.010 GeneticVariation BEFREE No correlation between rs873601 and rs2094258 and susceptibility to esophageal cancer</span> was found. 28952217

2019

dbSNP: rs2296147
rs2296147
0.010 GeneticVariation BEFREE The results of this case-control study showed that the polymorphic locus on ERCC5, rs2296147, could reduce the risk of esophageal cancer, which will help further understand the pathogenesis of esophageal cancer. 28952217

2019

dbSNP: rs315919
rs315919
0.010 GeneticVariation BEFREE Our study provided the first evidence that IL1RN rs3181052, rs452204, and rs315919 are correlated with a decreased risk of esophageal cancer in a Northwest Han Chinese population. 30995661

2019

dbSNP: rs3181052
rs3181052
0.010 GeneticVariation BEFREE In stratified analyses </span>by age >55 years, rs3181052 reduced the risk of esophageal cancer in the dominant and overdominant models. 30995661

2019

dbSNP: rs452204
rs452204
0.010 GeneticVariation BEFREE Our study provided the first evidence that IL1RN rs3181052, rs452204, and rs315919 are correlated with a decreased risk of esophageal cancer in a Northwest Han Chinese population. 30995661

2019

dbSNP: rs6720283
rs6720283
0.010 GeneticVariation BEFREE Stratified analysis was performed by gender, age, alcohol drinking, BMI, TNM stage and lymph node metastasis, the results showed that rs7436, rs115510139 and rs6720283 were significantly associated with the risk of EC in different groups (all p < 0.05). 31425922

2019

dbSNP: rs7436
rs7436
0.010 GeneticVariation BEFREE Stratified analysis was performed by gender, age, alcohol drinking, BMI, TNM stage and lymph node metastasis, the results showed that rs7436, rs115510139 and rs6720283 were significantly associated with the risk of EC in different groups (all p < 0.05). 31425922

2019

dbSNP: rs873601
rs873601
0.010 GeneticVariation BEFREE No correlation between rs873601 and rs2094258 and susceptibility to e</span>sophageal cancer was found. 28952217

2019

dbSNP: rs4767364
rs4767364
0.010 GeneticVariation BEFREE This study aims to investigate the relationship between ALDH2 rs671 and c12orf30 rs4767364 polymorphisms in the chromosome 12q24 gene, and risk and prognosis of individuals developing esophageal cancer (ESCC) in Xinjiang Kazak and Han populations. 28464297

2018

dbSNP: rs10069690
rs10069690
0.010 GeneticVariation BEFREE Of the four SNPs examined, rs10069690 and rs2242652 were correlated with esophageal cancer risk. 28060765

2017

dbSNP: rs11548103
rs11548103
0.010 GeneticVariation BEFREE <i>S100A14</i> rs11548103 G>A polymorphism is associated with a decreased risk of esophageal cancer in a Chinese population. 29156846

2017

dbSNP: rs174538
rs174538
0.010 GeneticVariation BEFREE Flap endonuclease-1 rs174538 G>A polymorphisms are associated with the risk of esophageal cancer in a Chinese population. 28319330

2017

dbSNP: rs2242652
rs2242652
0.010 GeneticVariation BEFREE Of the four SNPs examined, rs10069690 and rs2242652 were correlated with esophageal cancer risk. 28060765

2017

dbSNP: rs2244438
rs2244438
0.010 GeneticVariation BEFREE Four of the 20 SNPs identified as high-risk SNPs in Chinese esophageal cancer showed increased risk for Chinese lung cancer, which included rs3769823 (OR = 1.26; 95% CI = 1.107-1.509; P = 0.02), rs10931936 (OR = 1.283; 95% CI = 1.100-1.495; P = 0.04), rs2244438 (OR = 1.294; 95% CI = 1.098-1.525; P = 0.04) and rs13016963 (OR = 1.268; 95% CI = 1.089-1.447; P = 0.04). 28542283

2017

dbSNP: rs2320615
rs2320615
0.010 GeneticVariation BEFREE These results provide the first evidence that the rs2320615 in NAF1 was associated with reduced risk of esophageal cancer. 28454086

2017

dbSNP: rs3747093
rs3747093
0.010 GeneticVariation BEFREE Interestingly, we observed consistent associations between rs3747093 and multiple cancers (gastric cancer: OR = 0.85, P = 2.21 × 10<sup>-4</sup>; esophageal cancer: OR = 0.91, P = 2.57 × 10<sup>-2</sup>; colorectal cancer: OR = 0.80, P = 1.85 × 10<sup>-6</sup>; and breast cancer: OR = 0.87, P = 1.55 × 10<sup>-3</sup>). 28653172

2017

dbSNP: rs3856806
rs3856806
0.010 GeneticVariation BEFREE In a subgroup analysis by cancer type, <i>PPARG c.1347C>T</i> polymorphism was associated with risk of esophageal cancer and glioblastoma. 29254243

2017

dbSNP: rs895819
rs895819
0.010 GeneticVariation BEFREE In addition, no association was found between rs895819 and risk of gastric cancer or esophageal cancer. 29088869

2017