Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1057519996
rs1057519996
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: rs1057519997
rs1057519997
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: rs1057519997
rs1057519997
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: rs1057519997
rs1057519997
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: rs1057520002
rs1057520002
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: rs1057520002
rs1057520002
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: rs1057520003
rs1057520003
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: rs1057520004
rs1057520004
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: rs1057520004
rs1057520004
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: rs1057520007
rs1057520007
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: rs1057520007
rs1057520007
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: rs1057520007
rs1057520007
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: rs11540652
rs11540652
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: rs11540652
rs11540652
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: rs11540652
rs11540652
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: rs121912651
rs121912651
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: rs121912651
rs121912651
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: rs121912655
rs121912655
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: rs121912666
rs121912666
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: rs121912666
rs121912666
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: rs138729528
rs138729528
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: rs138729528
rs138729528
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: rs193920774
rs193920774
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: rs28934573
rs28934573
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: rs28934573
rs28934573
CUI: C0017636
Disease: Glioblastoma
Glioblastoma
A 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011

2016