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 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
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 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