Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs3748067
rs3748067
CUI: C0024623
Disease: Malignant neoplasm of stomach
Malignant neoplasm of stomach
0.080 GeneticVariation BEFREE The pooled estimate revealed an association between IL-17A rs2275913 polymorphism and the risk of GC under all genetic models (A vs. G, OR 1.187, 95% CI 1.086-1.297, P < 0.001; GA vs. GG, OR 1.108, 95% CI 1.008-1.218, P = 0.033; AA vs. GG, OR 1.484, 95% CI 1.236-1.781, P < 0.001), while no evidence of association was found with IL-17A rs3748067 or IL-17F rs763780 polymorphisms. 29860554

2018

dbSNP: rs3748067
rs3748067
CUI: C0024623
Disease: Malignant neoplasm of stomach
Malignant neoplasm of stomach
0.080 GeneticVariation BEFREE We found that CT (OR<sub>adj</sub> = 0.59; 95% CI: 0.44-0.79), CT + TT (OR<sub>adj</sub> = 0.58; 95% CI: 0.43-0.77) genotypes, and T allele (OR<sub>adj</sub> = 0.77; 95% CI: 0.47-0.80) of rs3748067 reduced GC risk; the rs10889677 CC genotype (OR<sub>adj</sub> = 2.22; 95% CI: 1.27-3.87) and C allele (OR<sub>adj</sub> = 1.24; 95% CI: 1.02-1.52) increased GC risk. 29118466

2017

dbSNP: rs3748067
rs3748067
CUI: C0024623
Disease: Malignant neoplasm of stomach
Malignant neoplasm of stomach
0.080 GeneticVariation BEFREE In conclusion, our results suggest that the IL-17A rs3748067C>T and IL-17F rs763780 T>C polymorphisms play an important role in the risk of gastric cancer in a Chinese population. 26535650

2015

dbSNP: rs3748067
rs3748067
CUI: C0024623
Disease: Malignant neoplasm of stomach
Malignant neoplasm of stomach
0.080 GeneticVariation BEFREE The rs2275913 AA (adjusted OR = 1.69, 95 % CI = 1.15-2.49) and rs3748067 TT (adjusted OR = 1.73, 95 % CI = 1.03-2.94) genotypes were associated with an increased risk of gastric cancer. 24218334

2014

dbSNP: rs3748067
rs3748067
CUI: C0024623
Disease: Malignant neoplasm of stomach
Malignant neoplasm of stomach
0.080 GeneticVariation BEFREE These results suggest that rs2275913 and rs3748067 variations significantly increase gastric cancer risk in a Chinese population. 25012243

2014

dbSNP: rs3748067
rs3748067
CUI: C0024623
Disease: Malignant neoplasm of stomach
Malignant neoplasm of stomach
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: rs3748067
rs3748067
CUI: C0024623
Disease: Malignant neoplasm of stomach
Malignant neoplasm of stomach
0.080 GeneticVariation BEFREE However, no significant positive signals were observed in the association analysis of the rs3748067 and rs763780 polymorphisms with the risk of gastric cancer in IL-17A and IL-17F, respectively. 25374195

2014

dbSNP: rs3748067
rs3748067
CUI: C0024623
Disease: Malignant neoplasm of stomach
Malignant neoplasm of stomach
0.080 GeneticVariation BEFREE In addition, rs2275913, rs3748067 and rs9382084 genetic variants were only associated with non-cardia gastric cancer. 24315816

2014

dbSNP: rs3748067
rs3748067
CUI: C0024623
Disease: Malignant neoplasm of stomach
Malignant neoplasm of stomach
0.080 GeneticVariation BEFREE The rs3748067 T polymorphism was associated with a decreased risk for intestinal GC (OR, 0.511; 95%CI, 0.272-0.962; p = 0.037), whereas rs2505901 C locus carried a decreased risk overall for GC (OR, 0.733; 95%CI, 0.545-0.985; p = 0.039). 22537748

2012