rs3856806, PPARG

N. diseases: 41
Disease: Esophageal Neoplasms ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Esophageal Neoplasms
CUI: C0014859
Disease: Esophageal Neoplasms
0.010 GeneticVariation BEFREE In a subgroup analysis by cancer type, <i>PPARG c.1347C>T</i> polymorphism was associated with risk of esophageal cancer and glioblastoma. 29254243 2017