Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs779221554
rs779221554
CUI: C1621958
Disease: Glioblastoma Multiforme
Glioblastoma Multiforme
0.700 GeneticVariation UNIPROT

dbSNP: rs770462360
rs770462360
CUI: C1621958
Disease: Glioblastoma Multiforme
Glioblastoma Multiforme
0.700 GeneticVariation UNIPROT

dbSNP: rs757496714
rs757496714
CUI: C1621958
Disease: Glioblastoma Multiforme
Glioblastoma Multiforme
0.700 GeneticVariation UNIPROT

dbSNP: rs375412266
rs375412266
CUI: C1621958
Disease: Glioblastoma Multiforme
Glioblastoma Multiforme
0.700 GeneticVariation UNIPROT

dbSNP: rs371854396
rs371854396
CUI: C1621958
Disease: Glioblastoma Multiforme
Glioblastoma Multiforme
0.700 GeneticVariation UNIPROT

dbSNP: rs17855787
rs17855787
CUI: C1621958
Disease: Glioblastoma Multiforme
Glioblastoma Multiforme
0.700 GeneticVariation UNIPROT

dbSNP: rs1567176006
rs1567176006
CUI: C1621958
Disease: Glioblastoma Multiforme
Glioblastoma Multiforme
G 0.700 GeneticVariation CLINVAR

dbSNP: rs1558650888
rs1558650888
CUI: C1621958
Disease: Glioblastoma Multiforme
Glioblastoma Multiforme
A 0.700 GeneticVariation CLINVAR

dbSNP: rs1466858740
rs1466858740
CUI: C1621958
Disease: Glioblastoma Multiforme
Glioblastoma Multiforme
0.700 GeneticVariation UNIPROT

dbSNP: rs1402272180
rs1402272180
CUI: C1621958
Disease: Glioblastoma Multiforme
Glioblastoma Multiforme
0.700 GeneticVariation UNIPROT

dbSNP: rs1384093596
rs1384093596
CUI: C1621958
Disease: Glioblastoma Multiforme
Glioblastoma Multiforme
0.700 GeneticVariation UNIPROT

dbSNP: rs7003908
rs7003908
CUI: C1621958
Disease: Glioblastoma Multiforme
Glioblastoma Multiforme
0.010 GeneticVariation BEFREE A 44% increase in risk for glioblastoma multiforme was found for individuals homozygous for the G allele of the PRKDC rs7003908 variant (odds ratio(GG), 1.44; 95% confidence interval, 1.13-1.84); there was a statistically significant trend (P = 0.009) with increasing number of G alleles. 19318434

2009

dbSNP: rs121913500
rs121913500
CUI: C1621958
Disease: Glioblastoma Multiforme
Glioblastoma Multiforme
0.100 GeneticVariation BEFREE A clonal IDH1 R132H mutation in the primary, a known GBM driver event, was detectable at only very low frequency in the recurrent tumour. 25732040

2015

dbSNP: rs55819519
rs55819519
CUI: C1621958
Disease: Glioblastoma Multiforme
Glioblastoma Multiforme
0.080 GeneticVariation BEFREE A clonal IDH1 R132H mutation in the primary, a known GBM driver event, was detectable at only very low frequency in the recurrent tumour. 25732040

2015

dbSNP: rs2017309
rs2017309
CUI: C1621958
Disease: Glioblastoma Multiforme
Glioblastoma Multiforme
0.010 GeneticVariation BEFREE A genetic polymorphism of the CHEK2 gene (CHEK2 SNP rs2017309 A/T) was genotyped in a series of glioblastoma patients (n = 213) and population controls (n = 192). 17016233

2006

dbSNP: rs8957
rs8957
CUI: C1621958
Disease: Glioblastoma Multiforme
Glioblastoma Multiforme
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: rs121913500
rs121913500
CUI: C1621958
Disease: Glioblastoma Multiforme
Glioblastoma Multiforme
0.100 GeneticVariation BEFREE A total of 15.3% of enrolled GBMs demonstrated loss of ATRX expression (ATRX-), 10.4% expressed an aberrant IDH1 R132H protein (IDH1+), and 48.4% exhibited p53 overexpression (p53+). 27478330

2016

dbSNP: rs55819519
rs55819519
CUI: C1621958
Disease: Glioblastoma Multiforme
Glioblastoma Multiforme
0.080 GeneticVariation BEFREE A total of 15.3% of enrolled GBMs demonstrated loss of ATRX expression (ATRX-), 10.4% expressed an aberrant IDH1 R132H protein (IDH1+), and 48.4% exhibited p53 overexpression (p53+). 27478330

2016

dbSNP: rs74315452
rs74315452
CUI: C1621958
Disease: Glioblastoma Multiforme
Glioblastoma Multiforme
0.010 GeneticVariation BEFREE Activation of caspase-1 and caspase-3 is observed also in neuroblastoma lines expressing other fALS-SOD1s (G37R, G85R, and I113T) cocultured with glioblastoma lines expressing the corresponding mutant enzymes. 15208263

2004

dbSNP: rs373584770
rs373584770
CUI: C1621958
Disease: Glioblastoma Multiforme
Glioblastoma Multiforme
0.010 GeneticVariation BEFREE Activation of caspase-1 and caspase-3 is observed also in neuroblastoma lines expressing other fALS-SOD1s (G37R, G85R, and I113T) cocultured with glioblastoma lines expressing the corresponding mutant enzymes. 15208263

2004

dbSNP: rs3851634
rs3851634
CUI: C1621958
Disease: Glioblastoma Multiforme
Glioblastoma Multiforme
T 0.710 GeneticVariation GWASCAT After genotyping an additional 1,490 cases and 1,723 controls we identify new risk loci for glioblastoma (GBM) at 12q23.33 (rs3851634, near POLR3B, P=3.02 × 10(-9)) and non-GBM at 10q25.2 (rs11196067, near VTI1A, P=4.32 × 10(-8)), 11q23.2 (rs648044, near ZBTB16, P=6.26 × 10(-11)), 12q21.2 (rs12230172, P=7.53 × 10(-11)) and 15q24.2 (rs1801591, near ETFA, P=5.71 × 10(-9)). 26424050

2015

dbSNP: rs3851634
rs3851634
CUI: C1621958
Disease: Glioblastoma Multiforme
Glioblastoma Multiforme
0.710 GeneticVariation BEFREE After genotyping an additional 1,490 cases and 1,723 controls we identify new risk loci for glioblastoma (GBM) at 12q23.33 (rs3851634, near POLR3B, P=3.02 × 10(-9)) and non-GBM at 10q25.2 (rs11196067, near VTI1A, P=4.32 × 10(-8)), 11q23.2 (rs648044, near ZBTB16, P=6.26 × 10(-11)), 12q21.2 (rs12230172, P=7.53 × 10(-11)) and 15q24.2 (rs1801591, near ETFA, P=5.71 × 10(-9)). 26424050

2015

dbSNP: rs11196067
rs11196067
CUI: C1621958
Disease: Glioblastoma Multiforme
Glioblastoma Multiforme
0.010 GeneticVariation BEFREE After genotyping an additional 1,490 cases and 1,723 controls we identify new risk loci for glioblastoma (GBM) at 12q23.33 (rs3851634, near POLR3B, P=3.02 × 10(-9)) and non-GBM at 10q25.2 (rs11196067, near VTI1A, P=4.32 × 10(-8)), 11q23.2 (rs648044, near ZBTB16, P=6.26 × 10(-11)), 12q21.2 (rs12230172, P=7.53 × 10(-11)) and 15q24.2 (rs1801591, near ETFA, P=5.71 × 10(-9)). 26424050

2015

dbSNP: rs1801591
rs1801591
CUI: C1621958
Disease: Glioblastoma Multiforme
Glioblastoma Multiforme
0.010 GeneticVariation BEFREE After genotyping an additional 1,490 cases and 1,723 controls we identify new risk loci for glioblastoma (GBM) at 12q23.33 (rs3851634, near POLR3B, P=3.02 × 10(-9)) and non-GBM at 10q25.2 (rs11196067, near VTI1A, P=4.32 × 10(-8)), 11q23.2 (rs648044, near ZBTB16, P=6.26 × 10(-11)), 12q21.2 (rs12230172, P=7.53 × 10(-11)) and 15q24.2 (rs1801591, near ETFA, P=5.71 × 10(-9)). 26424050

2015

dbSNP: rs648044
rs648044
CUI: C1621958
Disease: Glioblastoma Multiforme
Glioblastoma Multiforme
0.010 GeneticVariation BEFREE After genotyping an additional 1,490 cases and 1,723 controls we identify new risk loci for glioblastoma (GBM) at 12q23.33 (rs3851634, near POLR3B, P=3.02 × 10(-9)) and non-GBM at 10q25.2 (rs11196067, near VTI1A, P=4.32 × 10(-8)), 11q23.2 (rs648044, near ZBTB16, P=6.26 × 10(-11)), 12q21.2 (rs12230172, P=7.53 × 10(-11)) and 15q24.2 (rs1801591, near ETFA, P=5.71 × 10(-9)). 26424050

2015