Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs4880
rs4880
0.020 GeneticVariation BEFREE Val(16)Ala polymorphism is related to gastric cancer development. 20233853

2010

dbSNP: rs4986790
rs4986790
0.100 GeneticVariation BEFREE Asp299Gly and Thr399Ile polymorphisms in TLR4 have been associated with a variety of inflammatory and infectious conditions including gastric cancer. 24295404

2014

dbSNP: rs11671784
rs11671784
0.020 GeneticVariation BEFREE rs11671784 G/A and rs895819 A/G polymorphisms inversely affect gastric cancer susceptibility and miR-27a expression in a Chinese population. 25399405

2014

dbSNP: rs2910164
rs2910164
0.100 GeneticVariation BEFREE rs2910164 of miR-146a is associated with GC. 27267319

2016

dbSNP: rs2990245
rs2990245
0.010 GeneticVariation BEFREE rs2990245 is significantly associated with a decreased risk of GC. 30951202

2019

dbSNP: rs12416605
rs12416605
0.010 GeneticVariation BEFREE rs12416605:C>T in MIR938 associates with gastric cancer through affecting the regulation of the CXCL12 chemokine gene. 31273931

2019

dbSNP: rs8193
rs8193
0.010 GeneticVariation BEFREE rs8193 is statistically associated with the risk of malignancy, lymph node spread and stage of gastric cancer in Iranian population. 31376327

2020

dbSNP: rs8113645
rs8113645
0.010 GeneticVariation BEFREE A allele genotypes of rs8113645</span> and G allele genotypes of rs2288947 (rs8113645 GA and AA; rs2288947 AG and GG) were also significantly associated with decreased GC risk (p < 0.05). 27893425

2016

dbSNP: rs2288947
rs2288947
0.010 GeneticVariation BEFREE A allele genotypes of rs8113645 and G allele genotypes of rs2288947 (rs8113645 GA and AA; rs2288947 AG and GG) were also significantly associated with decreased GC risk (p < 0.05). 27893425

2016

dbSNP: rs10680577
rs10680577
0.010 GeneticVariation BEFREE A case-control study, including 415 GC patients and 830 healthy controls, was conducted to investigate the association between GC susceptibility with a 4-bp insertion/deletion polymorphism (rs10680577) in the proximal promoter of EGLN2. 24517638

2014

dbSNP: rs4719839
rs4719839
0.010 GeneticVariation BEFREE A functional genetic variant of miRNA rs4719839 and the corresponding haplotype were associated with clinicopathological features and prognosis of advanced GCs. 25261463

2014

dbSNP: rs1048943
rs1048943
0.030 GeneticVariation BEFREE A great number of studies regarding the association between MspI and Ile462Val polymorphisms in the CYP1A1 gene and gastric cancer have been published. 22359202

2012

dbSNP: rs1229984
rs1229984
0.020 GeneticVariation BEFREE A known functional SNP in ADH1B (rs1229984) was associated with alcohol intake (P-value = 0.04) but not GC risk. 22144473

2012

dbSNP: rs112754928
rs112754928
0.010 GeneticVariation BEFREE A low-frequency missense variant rs112754928 in the SPOC domain containing 1 gene (SPOCD1; encoding p.Arg71Trp), at 1p35.2, was reproducibly associated with reduced risk of gastric cancer (odds ratio, 0.56; P = 3.48 × 10<sup>-8</sup>). 28246015

2017

dbSNP: rs3748068
rs3748068
0.010 GeneticVariation BEFREE A meaningful interaction among ever smoked, family history of GC, and rs3748068 could intensify GC risk by 2.25-fold. 29118466

2017

dbSNP: rs74483926
rs74483926
0.010 GeneticVariation BEFREE A missense mutation (S3660L) in MLL3 gene influences risk of gastric cancer. 24965397

2014

dbSNP: rs744154
rs744154
0.020 GeneticVariation BEFREE A non-significant increased risk of gastric cancer was found in individuals carrying the rs744154 GG genotype. 23679285

2013

dbSNP: rs2274223
rs2274223
0.100 GeneticVariation BEFREE A notable signal was rs2274223, a nonsynonymous SNP located in PLCE1, for gastric cancer (P = 8.40 x 10(-9); per-allele odds ratio (OR) = 1.31) and ESCC (P = 3.85 x 10(-9); OR = 1.34). 20729852

2010

dbSNP: rs2910164
rs2910164
0.100 GeneticVariation BEFREE A significant association was found between rs2910164</span> and GC risk under all genetic models (CC vs. GG, OR = 0.76, 95% CI = 0.66-0.87; CC vs. GC+GG, OR = 0.84, 95% CI = 0.71-0.99; CC+GC vs. GG, OR = 0.82, 95% CI = 0.73-0.91) for the total data. 26202478

2017

dbSNP: rs3748067
rs3748067
0.080 GeneticVariation BEFREE A significant interaction was observed between the rs2275913G>A and rs3748067C>T genotype and subsites of gastric cancer (p for interaction of 0.044 and 0.008, respectively). 24218334

2014

dbSNP: rs920778
rs920778
0.040 GeneticVariation BEFREE A single nucleotide polymorphism (SNP) rs920778 in the HOTAIR gene, has been recurrently studied for susceptibility to many cancers including oesophageal cancer, gastric cancer, lung cancer, and hepatocellular carcinoma. 31759985

2020

dbSNP: rs13181
rs13181
0.090 GeneticVariation BEFREE A statistically significant finding could be seen in noncardia-type gastric cancer for XPD Lys751Gln polymorphism. 23028453

2012

dbSNP: rs671
rs671
0.070 GeneticVariation BEFREE A stratified analysis by country showed that the ALDH2 rs671 G>A polymorphism might be a risk factor for GC in Japan (Allele model: <i>P</i><sub>unadjusted</sub> = 0.034; Dominant model: <i>P</i><sub>unadjusted</sub> = 0.040); however, the result was nonsignificant when the Bonferroni correction and false discovery rate (FDR) were applied. 29254255

2017

dbSNP: rs12615966
rs12615966
0.010 GeneticVariation BEFREE Additionally, genetic model analyses showed that rs2689154 was associated with a reduced risk of GC</span> under the recessive model (adjusted OR = 0.46, 95% CI: 0.22-0.98, P = 0.037), and rs12615966 in FOXF1 was associated with an increased risk of GC in both the dominant and log-additive models after adjusted for age and gender (adjusted OR = 1.36, 95% CI: 1.02-1.81, P = 0.033; adjusted OR = 1.36, 95% CI: 1.05-1.75, P = 0.018, respectively). 28404937

2017

dbSNP: rs2689154
rs2689154
0.010 GeneticVariation BEFREE Additionally, genetic model analyses showed that rs2689154 was associated with a reduced risk of GC under the recessive model (adjusted OR = 0.46, 95% CI: 0.22-0.98, P = 0.037), and rs12615966 in FOXF1 was associated with an increased risk of GC in both the dominant and log-additive models after adjusted for age and gender (adjusted OR = 1.36, 95% CI: 1.02-1.81, P = 0.033; adjusted OR = 1.36, 95% CI: 1.05-1.75, P = 0.018, respectively). 28404937

2017