Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs121913500
rs121913500
0.800 GeneticVariation UNIPROT

dbSNP: rs121913499
rs121913499
0.720 GeneticVariation UNIPROT

dbSNP: rs104894156
rs104894156
0.700 GeneticVariation UNIPROT

dbSNP: rs1064794096
rs1064794096
0.700 GeneticVariation UNIPROT

dbSNP: rs1554893792
rs1554893792
0.700 GeneticVariation UNIPROT

dbSNP: rs63751110
rs63751110
0.700 GeneticVariation UNIPROT

dbSNP: rs786202398
rs786202398
0.700 GeneticVariation UNIPROT

dbSNP: rs1346787
rs1346787
0.030 GeneticVariation BEFREE <i>EFEMP1</i> rs1346787 polymorphism was significantly associated with glioma risk in Chinese population under all genetic models (GG vs AA, OR =2.22, 95% CI =1.46-3.36; AG vs AA, OR =1.54, 95% CI =1.27-1.87; (GG+AG) vs AA, OR =1.60, 95% CI =1.34-1.93; GG vs (AG+AA), OR =1.86, 95% CI =1.24-2.78; G vs A, OR =1.54, 95% CI =1.32-1.79). 29158681

2017

dbSNP: rs121913500
rs121913500
0.800 GeneticVariation BEFREE <i>IDH1</i> mutations only affected brainstem gliomas (6/24 vs 0/78; <i>p</i> = 7.5 × 10<sup>-5</sup>), were mostly non-R132H (contrasting with hemispheric gliomas, <i>p</i> = 0.0001), and were associated with longer survival (54 vs 12 months). 29728520

2018

dbSNP: rs1045485
rs1045485
0.020 GeneticVariation BEFREE D302H polymorphism of CASP8 gene may be associated with increased risk of glioma but larger study groups in different ethnic populations are needed to better elucidate the role of CASP8 gene polymorphism in the pathogenesis of primary brain tumors. 26359420

2016

dbSNP: rs113488022
rs113488022
0.100 GeneticVariation BEFREE A phase I/II clinical trial suggests that dabrafenib shrinks or stabilizes low-grade gliomas in children with the BRAF V600E mutation. 28062673

2017

dbSNP: rs121913377
rs121913377
0.100 GeneticVariation BEFREE A phase I/II clinical trial suggests that dabrafenib shrinks or stabilizes low-grade gliomas in children with the BRAF V600E mutation. 28062673

2017

dbSNP: rs498872
rs498872
0.900 GeneticVariation BEFREE A single nucleotide polymorphism (SNP) at locus 11q23.3 (rs498872) in the near 5'-UTR of the PHLDB1 gene was recently implicated as a risk factor for gliomas in a genome-wide association study, and this involvement was confirmed in three additional studies. 23300798

2012

dbSNP: rs25489
rs25489
0.090 GeneticVariation BEFREE A total of 11 studies (3,810 cases and 6,079 controls), 7 studies (2,928 cases and 5,048 controls), and 4 studies (1,461 cases and 2,593 controls) were finally included in the analyses of the association between XRCC1 Arg399Gln, Arg194Trp, and Arg280His polymorphisms and glioma risk, respectively. 23167420

2012

dbSNP: rs2289591
rs2289591
0.010 GeneticVariation BEFREE A variant in PER1 (rs2289591) was significantly associated with overall glioma risk (per variant allele OR 0.80; 95 % CI 0.66-0.97; p trend = 0.027). 24135790

2014

dbSNP: rs121913500
rs121913500
0.800 GeneticVariation BEFREE Activated leukocyte adhesion molecule expression in gliomas was independent of proliferative activity, MGMT status, patient survival, and age, whereas gliomas with IDH1 (R132H) mutation had significantly higher activated leukocyte adhesion molecule levels than their wild-type counterparts. 22304788

2012

dbSNP: rs121913500
rs121913500
0.800 GeneticVariation BEFREE Additionally, 5-aza enhances the therapeutic effect of the DNA damaging agent TMZ in both subcutaneous and orthotopic PDX models of IDH1 R132H mutant glioma. 30184215

2019

dbSNP: rs118101777
rs118101777
0.050 GeneticVariation BEFREE Additionally, 5-aza enhances the therapeutic effect of the DNA damaging agent TMZ in both subcutaneous and orthotopic PDX models of IDH1 R132H mutant glioma. 30184215

2019

dbSNP: rs7115578
rs7115578
0.010 GeneticVariation BEFREE Additionally, rs7115578 AG genotype represented a poorer prognosis of glioma (HR = 1.24, P=0.033) and astrocytoma (log-rank P=0.037, HR = 1.31, P=0.036). 31652449

2019

dbSNP: rs113488022
rs113488022
0.100 GeneticVariation BEFREE Additionally, BRAF V600E was only associated with a favorable prognosis in lower grade glioma. 28534272

2018

dbSNP: rs121913377
rs121913377
0.100 GeneticVariation BEFREE Additionally, BRAF V600E was only associated with a favorable prognosis in lower grade glioma. 28534272

2018

dbSNP: rs13181
rs13181
0.100 GeneticVariation BEFREE Additionally, subgroup analyses of 8 SNPs by ethnicity indicated that the mutation of rs13181, rs1800067 were apparently protective factors of glioma among Asians, while the mutation of rs13181 was a risk factors of glio</span>ma in Caucasians. 26843108

2017

dbSNP: rs1800067
rs1800067
0.060 GeneticVariation BEFREE Additionally, subgroup analyses of 8 SNPs by ethnicity indicated that the mutation of rs13181, rs1800067 were apparently protective factors of glioma among Asians, while the mutation of rs13181 was a risk factors of glioma in Caucasians. 26843108

2017

dbSNP: rs11979158
rs11979158
0.850 GeneticVariation BEFREE Additionally, subgroup analysis by stages of glioma found that variation of rs11979158 had stronger relationship with high-grade (OR = 1.32, 95 %CI = 1.19-1.45) than low-grade glioma (OR = 1.12, 95 % CI = 1.03-1.21). 26243184

2016

dbSNP: rs2236661
rs2236661
0.010 GeneticVariation BEFREE Additionally, two novel SNPs (rs2236661 and rs494560) that were independent of rs17749 were significantly associated with glioma risk in a recessive genetic model [P = 1.31×10⁻⁵ and P = 3.32×10⁻⁵, respectively]. 23300798

2012