Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs9694676
rs9694676
0.010 GeneticVariation BEFREE We observed a significant increase of the single nucleotide polymorphism (SNP) rs9694676 C-allele, located in the LRP12 promoter, in GGs compared to normal control individuals. 27142828

2016

dbSNP: rs113488022
rs113488022
0.100 GeneticVariation BEFREE We document two rare cases of massively metastatic spinal cord GGs in adult patients who were negative for BRAF V600E mutations via multiple methods. 25015869

2014

dbSNP: rs121913377
rs121913377
0.100 GeneticVariation BEFREE We document two rare cases of massively metastatic spinal cord GGs in adult patients who were negative for BRAF V600E mutations via multiple methods. 25015869

2014

dbSNP: rs113488022
rs113488022
0.100 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

dbSNP: rs121913377
rs121913377
0.100 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

dbSNP: rs1057519903
rs1057519903
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

dbSNP: rs113488022
rs113488022
0.100 GeneticVariation BEFREE VE1 immunostaining for BRAF(V600E) showed concordance with sequencing in nine of nine brainstem GGs including the two cases equivocal by Sanger. 24238153

2014

dbSNP: rs121913377
rs121913377
0.100 GeneticVariation BEFREE VE1 immunostaining for BRAF(V600E) showed concordance with sequencing in nine of nine brainstem GGs including the two cases equivocal by Sanger. 24238153

2014

dbSNP: rs113488022
rs113488022
0.100 GeneticVariation BEFREE Thus BRAF V600E mutation is common in desmoplastic non-infantile astrocytoma/ganglioglioma, but does not affect the prognosis. 29902580

2018

dbSNP: rs121913377
rs121913377
0.100 GeneticVariation BEFREE Thus BRAF V600E mutation is common in desmoplastic non-infantile astrocytoma/ganglioglioma, but does not affect the prognosis. 29902580

2018

dbSNP: rs113488022
rs113488022
0.100 GeneticVariation BEFREE Three gangliogliomas with BRAF p.V600E mutation had concurrent CDKN2A homozygous deletion and one additionally harbored a subclonal mutation in PTEN. 29880043

2018

dbSNP: rs121913377
rs121913377
0.100 GeneticVariation BEFREE Three gangliogliomas with BRAF p.V600E mutation had concurrent CDKN2A homozygous deletion and one additionally harbored a subclonal mutation in PTEN. 29880043

2018

dbSNP: rs113488022
rs113488022
0.100 GeneticVariation BEFREE These data suggest that BRAF V600E can predict the regrowth rate of brainstem gangliogliomas after microsurgery, and a BRAF V600E-targeted therapeutic may be a promising early intervention measure for patients who harbour BRAF V600E mutation after microsurgery. 28986151

2017

dbSNP: rs121913377
rs121913377
0.100 GeneticVariation BEFREE These data suggest that BRAF V600E can predict the regrowth rate of brainstem gangliogliomas after microsurgery, and a BRAF V600E-targeted therapeutic may be a promising early intervention measure for patients who harbour BRAF V600E mutation after microsurgery. 28986151

2017

dbSNP: rs113488022
rs113488022
0.100 GeneticVariation BEFREE The high mutation frequencies in pleomorphic xanthoastrocytomas, gangliogliomas and extra-cerebellar pilocytic astrocytomas implicate BRAF (V600E) mutation as a valuable diagnostic marker for these rare tumor entities. 21274720

2011

dbSNP: rs121913377
rs121913377
0.100 GeneticVariation BEFREE The high mutation frequencies in pleomorphic xanthoastrocytomas, gangliogliomas and extra-cerebellar pilocytic astrocytomas implicate BRAF (V600E) mutation as a valuable diagnostic marker for these rare tumor entities. 21274720

2011

dbSNP: rs113488022
rs113488022
0.100 GeneticVariation BEFREE The p.Val600Glu was found in 14/75 grade II GG.No EP were BRAF mutated. 31673897

2019

dbSNP: rs121913377
rs121913377
0.100 GeneticVariation BEFREE The p.Val600Glu was found in 14/75 grade II GG.No EP were BRAF mutated. 31673897

2019

dbSNP: rs113488022
rs113488022
0.100 GeneticVariation BEFREE Personalized Treatment for a Patient With a BRAF V600E Mutation Using Dabrafenib and a Tumor Treatment Fields Device in a High-Grade Glioma Arising From Ganglioglioma. 27799506

2016

dbSNP: rs121913377
rs121913377
0.100 GeneticVariation BEFREE Personalized Treatment for a Patient With a BRAF V600E Mutation Using Dabrafenib and a Tumor Treatment Fields Device in a High-Grade Glioma Arising From Ganglioglioma. 27799506

2016

dbSNP: rs113488022
rs113488022
0.100 GeneticVariation BEFREE PA and GG BRAF V600E-mutant had significantly lower rADCmean (p < 0.001) and rADCmin (p < 0.001) values than wild type, regardless of tumor histology and location. 31667545

2020

dbSNP: rs121913377
rs121913377
0.100 GeneticVariation BEFREE PA and GG BRAF V600E-mutant had significantly lower rADCmean (p < 0.001) and rADCmin (p < 0.001) values than wild type, regardless of tumor histology and location. 31667545

2020

dbSNP: rs113488022
rs113488022
0.100 GeneticVariation BEFREE Mutant BRAF V600E protein in ganglioglioma is predominantly expressed by neuronal tumor cells. 23435618

2013

dbSNP: rs121913377
rs121913377
0.100 GeneticVariation BEFREE Mutant BRAF V600E protein in ganglioglioma is predominantly expressed by neuronal tumor cells. 23435618

2013

dbSNP: rs113488022
rs113488022
0.100 GeneticVariation BEFREE In the third case, where the interval spanned multiple decades, the GG was found to be positive for both BRAF p.V600E immunohistochemistry (IHC) and for the KIAA1549-BRAF fusion. 31147230

2019