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