rs5275, PTGS2

N. diseases: 55
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Glioma
CUI: C0017638
Disease: Glioma
0.010 GeneticVariation BEFREE We found that the CC+CT genotype of rs5275 was common in the control group but not in the glioma group (P = 0.033). 25966079 2015