Source: BEFREE

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1057519903
rs1057519903
H3-3A
CUI: C1332969
Disease: Childhood Ganglioglioma
Childhood Ganglioglioma 		0.020 GeneticVariation BEFREE Here, we report a rare patient with spinal ganglioglioma carrying an H3 K27M mutation. 29675936

2018
dbSNP: rs1057519903
rs1057519903
H3-3A
CUI: C1332969
Disease: Childhood Ganglioglioma
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