rs13042395, SLC52A3

N. diseases: 13
Disease: Esophageal carcinoma ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Esophageal carcinoma
CUI: C0152018
Disease: Esophageal carcinoma
0.030 GeneticVariation BEFREE Significant associations were found between SLC52A3 rs13042395 polymorphism and decreased cancer risk among esophageal cancer, Asians, female, normal BMI and old age groups. 27600099 2016
Esophageal carcinoma
CUI: C0152018
Disease: Esophageal carcinoma
0.030 GeneticVariation BEFREE Two SNPs, rs753955 and rs13042395, were associated with the risk of non-cardia GC in different genetic models (p < 0.05).No SNPs were associated with EC. 26176862 2015
Esophageal carcinoma
CUI: C0152018
Disease: Esophageal carcinoma
0.030 GeneticVariation BEFREE However, there was no significant association between the C20orf54 rs13042395 genotype and esophageal cancer risk (adjusted OR = 0.99, 95 % CI = 0.63-1.57 for C20orf54 rs13042395 TT vs. CC). 22744421 2012