Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Childhood Ganglioglioma
CUI: C1332969
Disease: Childhood Ganglioglioma
0.020 GeneticVariation BEFREE We demonstrate in this first series of midline GGs that the H3 K27M mutation can occur in association with the BRAF V600E mutation in grade I glioneuronal tumors. 27984673 2018
Childhood Ganglioglioma
CUI: C1332969
Disease: Childhood Ganglioglioma
0.020 GeneticVariation BEFREE Here, we report a rare patient with spinal ganglioglioma carrying an H3 K27M mutation. 29675936 2018