Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs863224451
rs863224451
CUI: C0017636
Disease: Glioblastoma
Glioblastoma
A 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011

2016

dbSNP: rs786201057
rs786201057
CUI: C0017636
Disease: Glioblastoma
Glioblastoma
A 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011

2016

dbSNP: rs786201057
rs786201057
CUI: C0017636
Disease: Glioblastoma
Glioblastoma
C 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011

2016

dbSNP: rs78378222
rs78378222
CUI: C0017636
Disease: Glioblastoma
Glioblastoma
G 0.700 GeneticVariation GWASCAT Genome-wide association study of glioma subtypes identifies specific differences in genetic susceptibility to glioblastoma and non-glioblastoma tumors. 28346443

2017

dbSNP: rs78378222
rs78378222
CUI: C0017636
Disease: Glioblastoma
Glioblastoma
G 0.700 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: rs764146326
rs764146326
CUI: C0017636
Disease: Glioblastoma
Glioblastoma
G 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011

2016

dbSNP: rs764146326
rs764146326
CUI: C0017636
Disease: Glioblastoma
Glioblastoma
A 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011

2016

dbSNP: rs764146326
rs764146326
CUI: C0017636
Disease: Glioblastoma
Glioblastoma
T 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011

2016

dbSNP: rs747342068
rs747342068
CUI: C0017636
Disease: Glioblastoma
Glioblastoma
G 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011

2016

dbSNP: rs747342068
rs747342068
CUI: C0017636
Disease: Glioblastoma
Glioblastoma
C 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011

2016

dbSNP: rs730882025
rs730882025
CUI: C0017636
Disease: Glioblastoma
Glioblastoma
T 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011

2016

dbSNP: rs730882025
rs730882025
CUI: C0017636
Disease: Glioblastoma
Glioblastoma
A 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011

2016

dbSNP: rs730882008
rs730882008
CUI: C0017636
Disease: Glioblastoma
Glioblastoma
G 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011

2016

dbSNP: rs730882008
rs730882008
CUI: C0017636
Disease: Glioblastoma
Glioblastoma
T 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011

2016

dbSNP: rs730882005
rs730882005
CUI: C0017636
Disease: Glioblastoma
Glioblastoma
G 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011

2016

dbSNP: rs730882005
rs730882005
CUI: C0017636
Disease: Glioblastoma
Glioblastoma
T 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011

2016

dbSNP: rs730882005
rs730882005
CUI: C0017636
Disease: Glioblastoma
Glioblastoma
A 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011

2016

dbSNP: rs587782329
rs587782329
CUI: C0017636
Disease: Glioblastoma
Glioblastoma
G 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011

2016

dbSNP: rs587781525
rs587781525
CUI: C0017636
Disease: Glioblastoma
Glioblastoma
C 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011

2016

dbSNP: rs587781525
rs587781525
CUI: C0017636
Disease: Glioblastoma
Glioblastoma
A 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011

2016

dbSNP: rs587781525
rs587781525
CUI: C0017636
Disease: Glioblastoma
Glioblastoma
G 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011

2016

dbSNP: rs587780073
rs587780073
CUI: C0017636
Disease: Glioblastoma
Glioblastoma
G 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011

2016

dbSNP: rs587780073
rs587780073
CUI: C0017636
Disease: Glioblastoma
Glioblastoma
C 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011

2016

dbSNP: rs587780071
rs587780071
CUI: C0017636
Disease: Glioblastoma
Glioblastoma
A 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011

2016

dbSNP: rs587780070
rs587780070
CUI: C0017636
Disease: Glioblastoma
Glioblastoma
C 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011

2016