Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs13361707
rs13361707
CUI: C0024623
Disease: Malignant neoplasm of stomach
Malignant neoplasm of stomach
0.780 GeneticVariation BEFREE In similar, an increased risk of gastric cancer was also observed for rs13361707</span> TC genotype (adjusted OR = 1.47, 95%CI: 1.01-2.14, p = 0.043; additive model: adjusted OR = 1.22, 95%CI: 1.02-1.47, p = 0.033). 30253744

2018

dbSNP: rs13361707
rs13361707
CUI: C0024623
Disease: Malignant neoplasm of stomach
Malignant neoplasm of stomach
0.780 GeneticVariation BEFREE TLR1 rs4833095 SNP was associated with an increased risk of GC in a European population, while PRKAA1 rs13361707 genetic variant was not linked with GC. 30574617

2018

dbSNP: rs13361707
rs13361707
CUI: C0024623
Disease: Malignant neoplasm of stomach
Malignant neoplasm of stomach
0.780 GeneticVariation BEFREE The meta-analysis reveals that the PRKAA1 rs13361707 T>C polymorphism has a significant relationship with increased GC risk. 29620653

2018

dbSNP: rs13361707
rs13361707
CUI: C0024623
Disease: Malignant neoplasm of stomach
Malignant neoplasm of stomach
0.780 GeneticVariation BEFREE Correlation between protein kinase catalytic subunit alpha-1 gene rs13361707 polymorphism and gastric cancer susceptibility in asian populations. 28978122

2017

dbSNP: rs13361707
rs13361707
CUI: C0024623
Disease: Malignant neoplasm of stomach
Malignant neoplasm of stomach
0.780 GeneticVariation BEFREE In summary, these results indicated that the C allele of PRKAA1 rs13361707 was a low-penetrate risk factor for GCa. 26485766

2015

dbSNP: rs13361707
rs13361707
CUI: C0024623
Disease: Malignant neoplasm of stomach
Malignant neoplasm of stomach
0.780 GeneticVariation BEFREE In the dominant model, SNPs rs13361707 [odds ratio (OR) = 1.51, 95%CI: 1.07-2.11)], rs154268 (OR = 1.65, 95%CI: 1.22-2.22), rs6882903 (OR = 1.48, 95%CI: 1.09-2.00), and rs10074991 (OR = 1.53, 95%CI: 1.09-2.16) were significantly associated with an increased risk of gastric cancer. 25024613

2014

dbSNP: rs13361707
rs13361707
CUI: C0024623
Disease: Malignant neoplasm of stomach
Malignant neoplasm of stomach
0.780 GeneticVariation BEFREE These findings indicate that the three SNPs (rs4072037, rs13361707 and rs2274223) identified in the GWASs may interact with H. pylori infection to increase the risk of GC. 24069371

2013

dbSNP: rs13361707
rs13361707
CUI: C0024623
Disease: Malignant neoplasm of stomach
Malignant neoplasm of stomach
0.780 GeneticVariation BEFREE Our study showed that the rs13361707 polymorphism was associated with increased risk of gastric cancer in a Korean population. 23861218

2013

dbSNP: rs13361707
rs13361707
CUI: C0024623
Disease: Malignant neoplasm of stomach
Malignant neoplasm of stomach
0.780 GeneticVariation GWASDB We identified two new susceptibility loci for non-cardia gastric cancer at 5p13.1 (rs13361707 in the region including PTGER4 and PRKAA1; odds ratio (OR) = 1.41; P = 7.6 × 10(-29)) and 3q13.31 (rs9841504 in ZBTB20; OR = 0.76; P = 1.7 × 10(-9)). 22037551

2011

dbSNP: rs9841504
rs9841504
CUI: C0024623
Disease: Malignant neoplasm of stomach
Malignant neoplasm of stomach
0.720 GeneticVariation BEFREE Those subjects with both the risk alleles MUC1 rs9841504 and ZBTB20 rs4072037 had a greater than 3-fold increased risk of gastric cancer. 27127881

2016

dbSNP: rs9841504
rs9841504
CUI: C0024623
Disease: Malignant neoplasm of stomach
Malignant neoplasm of stomach
0.720 GeneticVariation BEFREE However, we found no association between rs9841504 and gastric cancer risk. 23861218

2013

dbSNP: rs9841504
rs9841504
CUI: C0024623
Disease: Malignant neoplasm of stomach
Malignant neoplasm of stomach
0.720 GeneticVariation GWASDB We identified two new susceptibility loci for non-cardia gastric cancer at 5p13.1 (rs13361707 in the region including PTGER4 and PRKAA1; odds ratio (OR) = 1.41; P = 7.6 × 10(-29)) and 3q13.31 (rs9841504 in ZBTB20; OR = 0.76; P = 1.7 × 10(-9)). 22037551

2011

dbSNP: rs1371429276
rs1371429276
CUI: C0024623
Disease: Malignant neoplasm of stomach
Malignant neoplasm of stomach
0.700 GeneticVariation UNIPROT

dbSNP: rs63749803
rs63749803
CUI: C0024623
Disease: Malignant neoplasm of stomach
Malignant neoplasm of stomach
0.700 GeneticVariation UNIPROT

dbSNP: rs63750297
rs63750297
CUI: C0024623
Disease: Malignant neoplasm of stomach
Malignant neoplasm of stomach
0.700 GeneticVariation UNIPROT

dbSNP: rs63750623
rs63750623
CUI: C0024623
Disease: Malignant neoplasm of stomach
Malignant neoplasm of stomach
0.700 GeneticVariation UNIPROT

dbSNP: rs63750709
rs63750709
CUI: C0024623
Disease: Malignant neoplasm of stomach
Malignant neoplasm of stomach
0.700 GeneticVariation UNIPROT

dbSNP: rs63750795
rs63750795
CUI: C0024623
Disease: Malignant neoplasm of stomach
Malignant neoplasm of stomach
0.700 GeneticVariation UNIPROT

dbSNP: rs63750966
rs63750966
CUI: C0024623
Disease: Malignant neoplasm of stomach
Malignant neoplasm of stomach
0.700 GeneticVariation UNIPROT

dbSNP: rs63751047
rs63751047
CUI: C0024623
Disease: Malignant neoplasm of stomach
Malignant neoplasm of stomach
0.700 GeneticVariation UNIPROT

dbSNP: rs63751400
rs63751400
CUI: C0024623
Disease: Malignant neoplasm of stomach
Malignant neoplasm of stomach
0.700 GeneticVariation UNIPROT

dbSNP: rs768678989
rs768678989
MET
CUI: C0024623
Disease: Malignant neoplasm of stomach
Malignant neoplasm of stomach
0.700 GeneticVariation UNIPROT

dbSNP: rs771333219
rs771333219
MET
CUI: C0024623
Disease: Malignant neoplasm of stomach
Malignant neoplasm of stomach
0.700 GeneticVariation UNIPROT

dbSNP: rs780759537
rs780759537
CUI: C0024623
Disease: Malignant neoplasm of stomach
Malignant neoplasm of stomach
0.700 GeneticVariation UNIPROT

dbSNP: rs1042522
rs1042522
CUI: C0024623
Disease: Malignant neoplasm of stomach
Malignant neoplasm of stomach
0.100 GeneticVariation BEFREE In the case-control study, rs1042522 (<i>TP53</i>) was associated with a stronger risk for developing gastric cancer in the sample stratified for diffuse subtype patients when compared to the risk observed for the total cases; CTC haplotype (rs699947/rs833061/rs2010963 <i>VEGFA</i>) was associated with risk while rs699947 was associated with protection for gastric malignancy in the total sample. 30551681

2018