rs11552822
|
|
|
0.700 |
GeneticVariation |
UNIPROT |
|
|
|
rs747621669
|
|
|
0.700 |
GeneticVariation |
UNIPROT |
|
|
|
rs1800629
|
|
|
0.020 |
GeneticVariation |
BEFREE |
<b>Background</b>: TNF-α-308G/A (rs1800629) polymorphism has been previously implicated in the susceptibility to esophageal cancer, but results of these studies remained controversial or ambiguous.
|
30854115 |
2019 |
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 |
rs1052133
|
|
|
0.030 |
GeneticVariation |
BEFREE |
Ser326Cys polymorphism in hOGG1 gene and risk of esophageal cancer in a Chinese population.
|
11307145 |
2001 |
rs61748181
|
|
|
0.010 |
GeneticVariation |
BEFREE |
A279T induces telomere dysfunction and inhibits non-canonical telomerase activity in esophageal cancer cells.
|
24983628 |
2014 |
rs1217691063
|
|
|
0.100 |
GeneticVariation |
BEFREE |
A meta-analysis was performed to obtain summary estimated odd ratios and 95% confidence intervals of folate intake and MTHFR C677T for esophageal cancer.
|
21517266 |
2011 |
rs4462560
|
|
|
0.010 |
GeneticVariation |
BEFREE |
A NEIL1 single nucleotide polymorphism (rs4462560) predicts the risk of radiation-induced toxicities in esophageal cancer patients treated with definitive radiotherapy.
|
24022861 |
2013 |
rs3765524
|
|
T |
0.820 |
GeneticVariation |
GWASDB |
A shared susceptibility locus in PLCE1 at 10q23 for gastric adenocarcinoma and esophageal squamous cell carcinoma.
|
20729852 |
2010 |
rs3765524
|
|
T |
0.820 |
GeneticVariation |
GWASCAT |
A shared susceptibility locus in PLCE1 at 10q23 for gastric adenocarcinoma and esophageal squamous cell carcinoma.
|
20729852 |
2010 |
rs738722
|
|
T |
0.810 |
GeneticVariation |
GWASCAT |
A shared susceptibility locus in PLCE1 at 10q23 for gastric adenocarcinoma and esophageal squamous cell carcinoma.
|
20729852 |
2010 |
rs738722
|
|
T |
0.810 |
GeneticVariation |
GWASDB |
A shared susceptibility locus in PLCE1 at 10q23 for gastric adenocarcinoma and esophageal squamous cell carcinoma.
|
20729852 |
2010 |
rs3781264
|
|
C |
0.700 |
GeneticVariation |
GWASDB |
A shared susceptibility locus in PLCE1 at 10q23 for gastric adenocarcinoma and esophageal squamous cell carcinoma.
|
20729852 |
2010 |
rs4072037
|
|
A |
0.700 |
GeneticVariation |
GWASDB |
A shared susceptibility locus in PLCE1 at 10q23 for gastric adenocarcinoma and esophageal squamous cell carcinoma.
|
20729852 |
2010 |
rs2274223
|
|
|
0.900 |
GeneticVariation |
BEFREE |
A single-nucleotide polymorphism (rs2274223: A5780G:His1927Arg) in the phospholipase C epsilon gene (PLCϵ) was recently identified as a susceptibility locus for esophageal cancer in Chinese subjects.
|
23390063 |
2013 |
rs1229984
|
|
|
0.840 |
GeneticVariation |
BEFREE |
ADH1B Arg47His polymorphism is associated with esophageal cancer risk in high-incidence Asian population: evidence from a meta-analysis.
|
21048924 |
2010 |
rs201745983
|
|
|
0.010 |
GeneticVariation |
BEFREE |
ADH1B Arg47His polymorphism is associated with esophageal cancer risk in high-incidence Asian population: evidence from a meta-analysis.
|
21048924 |
2010 |
rs1217691063
|
|
|
0.100 |
GeneticVariation |
BEFREE |
ALDH2, MTHFR C677T, CYP1A1 Ile/Val, CYP1A1MspI, CYP2E1, GSTP1, GSTM1 and GSTT1 were examined by meta-analyses and significant relations were found between ALDH2*1*2 and the CYP1A1 Val allele and increased risk of esophageal cancer.
|
17674367 |
2007 |
rs879253942
|
|
|
0.010 |
GeneticVariation |
BEFREE |
ALDH2, MTHFR C677T, CYP1A1 Ile/Val, CYP1A1MspI, CYP2E1, GSTP1, GSTM1 and GSTT1 were examined by meta-analyses and significant relations were found between ALDH2*1*2 and the CYP1A1 Val allele and increased risk of esophageal cancer.
|
17674367 |
2007 |
rs13181
|
|
|
0.020 |
GeneticVariation |
BEFREE |
Although no significant risk associations were observed for rs13181, further mini meta-analysis with our and 18 other published studies of 5,012 cases and 8,238 controls found evidence of an association between the rs13181 variant G allele and esophageal cancer risk (TG/GG vs. TT, OR = 1.17; 95% CI = 1.02-1.33).
|
25209371 |
2014 |
rs671
|
|
|
0.880 |
GeneticVariation |
BEFREE |
Among male daily consumers, the HRs (95% CIs) for EC associated with 15g/d of alcohol were 1.28 (1.15, 1.44) for "soon" response [vs. other responses: 1.12 (1.09, 1.15); p<sub>interaction</sub> = 0.047; n = 36,401, 425 EC cases] and 1.41 (1.08, 1.82) for rs671 GA [vs. GG: 1.16 (1.06, 1.27); p<sub>interaction</sub> = 0.493; n = 6,607, 80 EC cases].
|
29707772 |
2018 |
rs1042522
|
|
|
0.080 |
GeneticVariation |
BEFREE |
Among the five TP53 polymorphisms investigated, only p.R72P polymorphism may contributes to EC susceptibility.
|
25339039 |
2014 |
rs1131691014
|
|
|
0.070 |
GeneticVariation |
BEFREE |
Among the five TP53 polymorphisms investigated, only p.R72P polymorphism may contributes to EC susceptibility.
|
25339039 |
2014 |
rs878854066
|
|
|
0.070 |
GeneticVariation |
BEFREE |
Among the five TP53 polymorphisms investigated, only p.R72P polymorphism may contributes to EC susceptibility.
|
25339039 |
2014 |
rs6214
|
|
|
0.010 |
GeneticVariation |
BEFREE |
An OR of 1.54 (95% CI, 1.05-2.27) was found for EC for genotype AA of rs6214.
|
24608110 |
2014 |