Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs121434254
rs121434254
0.010 GeneticVariation BEFREE Heterozygous mutations of AIRE were identified in 3 patients: a patient with PBC and a patient with AIH type 1 carried a R257X mutation, and a patient with AIH type 2, diabetes mellitus type 1 (IDDM), thyroid disease, and atrophic gastritis carried a G305S mutation in the first PHD ring finger domain of the AIRE protein. 11343230

2001

dbSNP: rs1440526066
rs1440526066
0.010 GeneticVariation BEFREE On the other hand, homozygotes with the low activity allele of the A398G polymorphism in the IL4R gene had a modest increase in risk of atrophic gastritis (OR = 1.52, 95% CI: 1.05-2.21), compared with homozygotes of the high activity allele. 17006724

2006

dbSNP: rs764097618
rs764097618
0.010 GeneticVariation BEFREE On the other hand, homozygotes with the low activity allele of the A398G polymorphism in the IL4R gene had a modest increase in risk of atrophic gastritis (OR = 1.52, 95% CI: 1.05-2.21), compared with homozygotes of the high activity allele. 17006724

2006

dbSNP: rs765803011
rs765803011
0.010 GeneticVariation BEFREE On the other hand, homozygotes with the low activity allele of the A398G polymorphism in the IL4R gene had a modest increase in risk of atrophic gastritis (OR = 1.52, 95% CI: 1.05-2.21), compared with homozygotes of the high activity allele. 17006724

2006

dbSNP: rs2297518
rs2297518
0.010 GeneticVariation BEFREE A nonsynonymous SNP of NOS2A (Ser608Leu) and an SNP located in the promoter of IFNGR1 (C-56T) were associated with higher risk of atrophic gastritis [odds ratio (OR)=1.37, 95% confidence interval (CI)=1.01-1.86, and OR=1.49, 95% CI=1.01-2.19, respectively]. 18287876

2008

dbSNP: rs4986791
rs4986791
0.010 GeneticVariation BEFREE TLR4/D299G/T399I polymorphisms were more frequent in duodenal ulcer and showed a trend in gastric cancer, when compared with non-atrophic gastritis. 18755634

2008

dbSNP: rs2301756
rs2301756
0.020 GeneticVariation BEFREE This study aimed to examine the formerly reported association of G/A PTPN11 (protein-tyrosine phosphatase, nonreceptor-type 11) polymorphism (rs2301756) with gastric atrophy, as well as the association with gastric cancer in a Japanese population using a large sample size. 19589142

2009

dbSNP: rs2301756
rs2301756
0.020 GeneticVariation BEFREE Our previous studies found the AA genotype of a G/A single nucleotide polymorphism at intron 3 (rs2301756) of PTPN11 gene, which encodes SHP-2, to be associated with a lower risk of gastric atrophy. 18712962

2009

dbSNP: rs6672420
rs6672420
0.010 GeneticVariation BEFREE We found no statistically significant associations between RUNX3 rs6672420 polymorphism and risk of gastric atrophy, nor between these two RUNX3 polymorphisms and the risk of gastric cancer relative to the subjects with gastric atrophy. 19728008

2009

dbSNP: rs760805
rs760805
0.010 GeneticVariation BEFREE Significant association of RUNX3 T/A polymorphism at intron 3 (rs760805) with the risk of gastric atrophy in Helicobacter pylori seropositive Japanese. 19728008

2009

dbSNP: rs1052133
rs1052133
0.010 GeneticVariation BEFREE To investigate the association between Ser326Cys human oxoguanine glycosylase 1 (hOGG1) polymorphism and atrophic gastritis and gastric cancer after Helicobacter pylori (H. pylori) eradication. 20845517

2010

dbSNP: rs3805246
rs3805246
0.010 GeneticVariation BEFREE We could not confirm a major association between Gab1 SNP (rs3805246) and the predisposition to H. pylori infection and CAG in this study population from Germany. 20602450

2010

dbSNP: rs2910164
rs2910164
0.010 GeneticVariation BEFREE This study revealed the combined effect of miR-146a rs2910164 G/G and TLR4 +3725 C allele on the increased risk of severe gastric atrophy among the H. pylori-infected Japanese subjects. 20721625

2011

dbSNP: rs12423190
rs12423190
0.010 GeneticVariation BEFREE Our study provides the first evidence that rs12423190 polymorphism of the PTPN11 gene is significantly associated with an increased risk of gastric atrophy in H. pylori infected Chinese Han population, suggesting that rs12423190 polymorphism could be used as a useful marker of genetic susceptibility to gastric atrophy among H. pylori infected subjects. 22788847

2012

dbSNP: rs2014486
rs2014486
0.010 GeneticVariation BEFREE We genotyped MUC1 T31T, MUC2 L58P, MUC2 V116M, MUC5B E34G, MUC5B R51W, MUC5B rs2014486 (intronic) and MUC6 V619M for 533 serologically defined CAG cases and 1054 age- and sex-matched controls. 21596555

2012

dbSNP: rs7481521
rs7481521
0.010 GeneticVariation BEFREE We genotyped MUC1 T31T, MUC2 L58P, MUC2 V116M, MUC5B E34G, MUC5B R51W, MUC5B rs2014486 (intronic) and MUC6 V619M for 533 serologically defined CAG cases and 1054 age- and sex-matched controls. 21596555

2012

dbSNP: rs2294008
rs2294008
PSCA ; JRK
0.720 GeneticVariation BEFREE The T allele of rs2294008 was found to be associated with a higher prevalence of atrophic gastritis (OR = 1.44; 95% CI 1.03-2.01 for the dominant model) and intestinal metaplasia (OR = 1.50; 95% CI 1.13-1.98 for the dominant model). 24023815

2013

dbSNP: rs6458238
rs6458238
PGC
0.040 GeneticVariation BEFREE In gastric cancerous specimens, we observed significantly higher messenger RNA level in the subjects carrying the PGC rs6458238 GA genotype than that in subjects with the common GG genotype. 23455381

2013

dbSNP: rs1042194
rs1042194
0.010 GeneticVariation BEFREE SNPs rs9315542 (UFM1 gene), rs6878265 (THBS4 gene), rs1042194 (CYP2C19 gene) and rs10505799 (MGST1 gene) were significantly associated with atrophic gastritis, complete intestinal metaplasia, incomplete metaplasia with foci of dysplasia and dysplasia, respectively. 23801863

2013

dbSNP: rs10505799
rs10505799
0.010 GeneticVariation BEFREE SNPs rs9315542 (UFM1 gene), rs6878265 (THBS4 gene), rs1042194 (CYP2C19 gene) and rs10505799 (MGST1 gene) were significantly associated with atrophic gastritis, complete intestinal metaplasia, incomplete metaplasia with foci of dysplasia and dysplasia, respectively. 23801863

2013

dbSNP: rs12229892
rs12229892
0.010 GeneticVariation BEFREE We observed that PGC rs6458238, PGC rs4711690 and PTPN11 rs12229892 were associated with susceptibilities to GA and/or GC. 23455381

2013

dbSNP: rs254942
rs254942
0.010 GeneticVariation BEFREE Our findings suggested that the ERCC4 rs6498486 and rs254942 may be associated with AG risk. 23415627

2013

dbSNP: rs3814896
rs3814896
0.010 GeneticVariation BEFREE To our knowledge, this is the first report of an association between the TFF2 rs3814896 AG+GG genotypes and decreased risks of GC, diffuse-type GC, and atrophic gastritis in younger people aged ≤ 50 years, and an association between TFF3 rs9981660 AG+AA genotype and decreased risk of diffuse-type GC in men. 23933418

2013

dbSNP: rs4711690
rs4711690
PGC
0.010 GeneticVariation BEFREE We observed that PGC rs6458238, PGC rs4711690 and PTPN11 rs12229892 were associated with susceptibilities to GA and/or GC. 23455381

2013

dbSNP: rs6498486
rs6498486
0.010 GeneticVariation BEFREE Our findings suggested that the ERCC4 rs6498486 and rs254942 may be associated with AG risk. 23415627

2013