Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs9933544
rs9933544
0.010 GeneticVariation BEFREE Stratification analyses revealed that rs2033214 was only significantly associated with low-grade gliomas; rs9933544 and rs13332653 were only significantly associated with glioblastoma multiforme; and rs11860248 was significantly associated with both low-grade gliomas and glioblastoma multiforme, compared with the common wild-type homozygous genotype. 25127414

2014

dbSNP: rs9642393
rs9642393
0.010 GeneticVariation BEFREE When we analyzed tSNPs under different inheritance models, we found rs9642393 in EGFR increased odds of developing GBM in the dominant model. 24005813

2013

dbSNP: rs8957
rs8957
0.010 GeneticVariation BEFREE A missense variant, rs8957 (E[GAG]233D[GAU], SLC2A4RG, 20q13.33), was found being associated with GBM risk, with an odd ratio (OR) of 1.43 (95% confidence interval (CI) = 1.25-1.64, <i>P</i> = 1.72E-07). 28979815

2017

dbSNP: rs891835
rs891835
0.020 GeneticVariation BEFREE We identified LIG4 rs7325927 and BTBD2 rs11670188 as predictors of STS in GBM and CCDC26 rs10464870 and rs891835, HMGA2 rs1563834, and RTEL1 rs2297440 as predictors of LTS. 20368557

2010

dbSNP: rs891835
rs891835
0.020 GeneticVariation BEFREE We found rs891835 in CCDC26 to be associated with GBM susceptibility at a level of p=0.009. 24870769

2014

dbSNP: rs879254044
rs879254044
0.010 GeneticVariation BEFREE In this report, we present the case of a 5-year-old female with GBM and CMMRD due to an <i>MSH6</i> homozygous c.1883G>A mutation, who continues to experience an exceptional and durable response (9 months) to the immune checkpoint inhibitor (ICPI) nivolumab. 30104292

2018

dbSNP: rs878854066
rs878854066
0.010 GeneticVariation BEFREE Our study suggests that the polymorphism of p53 codon 72 Arg/Pro may play a protective role in the development of glioblastoma. 23860773

2013

dbSNP: rs865880036
rs865880036
0.010 GeneticVariation BEFREE Gene expression profiles of three glioma stem cell line samples, three normal astrocyte samples, three astrocyte overexpressing 4 iPSC-inducing and oncogenic factors (myc(T58A), OCT-4, p53DD, and H-Ras(G12V)) samples, three astrocyte overexpressing 7 iPSC-inducing and oncogenic factors (OCT4, H-Ras(G12V), myc(T58A), p53DD, cyclin D1, CDK4(RC24) and hTERT) samples and three glioblastoma cell line samples were downloaded from the ArrayExpress database (accession: E-MTAB-4771). 28952134

2017

dbSNP: rs863225401
rs863225401
0.010 GeneticVariation BEFREE In this report, we present the case of a 5-year-old female with GBM and CMMRD due to an <i>MSH6</i> homozygous c.1883G>A mutation, who continues to experience an exceptional and durable response (9 months) to the immune checkpoint inhibitor (ICPI) nivolumab. 30104292

2018

dbSNP: rs861539
rs861539
0.030 GeneticVariation BEFREE Genotypic and allelic frequencies of seven common polymorphisms in DNA repair genes involved in nucleotide excision repair (ERCC1 rs11615, ERCC2 rs13181, ERCC6 rs4253079), base excision repair (APEX1 rs1130409, XRCC1 rs25487), double-strand break repair (XRCC3 rs861539) and mismatch repair (MLH1 rs1800734) pathways were analyzed in 115 glioblastoma patients and 200 healthy controls. 24325908

2014

dbSNP: rs861539
rs861539
0.030 GeneticVariation BEFREE We examined XRCC3 Thr241Met polymorphism using PCR-RFLP in 80 astrocytoma and glioblastoma samples. 22370935

2012

dbSNP: rs861539
rs861539
0.030 GeneticVariation BEFREE Moreover, RAD51 rs1801320 C allele increased the risk to develop glioblastoma also when combined to XRCC1 rs25487 G allele and XRCC3 rs861539 C allele (χ(2) = 6.558; p = 0.0053). 26511493

2016

dbSNP: rs833061
rs833061
0.010 GeneticVariation BEFREE The VEGF polymorphism rs833061 was strongly associated with increased risk for glioma (odds ratio = 164.85) and glioblastoma (odds ratio = 155.66), confirmed after Bonferroni correction. 29584591

2018

dbSNP: rs8057643
rs8057643
0.010 GeneticVariation BEFREE In group 2, only one of the 16 SNPs, rs8057643 (located on 16p13.2), was significantly associated with glioblastoma age at diagnosis (nominal P = 0.0017; Bonferroni corrected P = 0.054). 17200355

2007

dbSNP: rs78378222
rs78378222
G 0.710 GeneticVariation GWASCAT Age-specific genome-wide association study in glioblastoma identifies increased proportion of 'lower grade glioma'-like features associated with younger age. 30152087

2018

dbSNP: rs78378222
rs78378222
0.710 GeneticVariation BEFREE The association between rs78378222 and risk was seen for both glioblastoma multiforme (GBM) and non-GBM tumours. 23571737

2013

dbSNP: rs78378222
rs78378222
G 0.710 GeneticVariation GWASCAT Genome-wide association study of glioma subtypes identifies specific differences in genetic susceptibility to glioblastoma and non-glioblastoma tumors. 28346443

2017

dbSNP: rs781490101
rs781490101
0.010 GeneticVariation BEFREE On the other hand, the Nuclear factor of activated T-cells (NFAT)-luciferase reporter was more potently activated by p53-K120R than by wild-type p53 and other mutants in glioblastoma, hepatoma and esophageal carcinoma cells. 19416725

2009

dbSNP: rs779221554
rs779221554
0.700 GeneticVariation UNIPROT

dbSNP: rs77724903
rs77724903
RET
0.010 GeneticVariation BEFREE Sequencing of exon 13 identified mutation c.2372A>T in codon 791 (Y791F) in heterozygous state in one of 100 GBM patients, in two of 65 patients with gastric cancer, in two of 54 PDAC patients and in none of the controls. 21311890

2011

dbSNP: rs774238794
rs774238794
0.010 GeneticVariation BEFREE The R132H mutation in isocitrate dehydrogenase 1 (IDH1<sup>R132H</sup>) is commonly observed and associated with better survival in glioblastoma multiforme (GBM), a malignant brain tumor. 31151327

2019

dbSNP: rs7732320
rs7732320
T 0.700 GeneticVariation GWASCAT SSBP2 variants are associated with survival in glioblastoma patients. 22472174

2012

dbSNP: rs771563543
rs771563543
0.010 GeneticVariation BEFREE Mean CBF1 expression is significantly increased in isocitrate dehydrogenase 1 (IDH1) R132H mutant glioblastoma and serves as prognostic marker for prolonged overall survival in brain tumours, particularly after therapy with temozolomide. 28571041

2017

dbSNP: rs770462360
rs770462360
0.700 GeneticVariation UNIPROT

dbSNP: rs769809364
rs769809364
0.010 GeneticVariation BEFREE We found that zinc re-established chemosensitivity in breast cancer SKBR3 (expressing R175H mutation) and glioblastoma U373MG (expressing R273H mutation) cell lines. 21508668

2011