rs121913500, IDH1

N. diseases: 96
Disease: Newly Diagnosed Childhood Ependymoma ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Newly Diagnosed Childhood Ependymoma
CUI: C0796611
Disease: Newly Diagnosed Childhood Ependymoma
0.010 GeneticVariation BEFREE As the presence of the p.R132H mutation in the IDH1 gene seems to be a more powerful prognostic marker than O(6)-methylguanine-DNA methyltransferase promoter status, we evaluated the presence of IDH1 mutation in Polish patients with astrocytoma, glioblastoma, oligoastrocytoma, ganglioglioma, oligodendroglioma, and ependymoma. 23934769 2014