Source: CLINVAR

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs121912666
rs121912666
CUI: C0006118
Disease: Brain Neoplasms
Brain Neoplasms
G 0.800 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011

2016

dbSNP: rs121912666
rs121912666
CUI: C0006118
Disease: Brain Neoplasms
Brain Neoplasms
C 0.800 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011

2016

dbSNP: rs121913343
rs121913343
CUI: C0006118
Disease: Brain Neoplasms
Brain Neoplasms
T 0.710 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011

2016

dbSNP: rs985033810
rs985033810
CUI: C0006118
Disease: Brain Neoplasms
Brain Neoplasms
T 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011

2016

dbSNP: rs985033810
rs985033810
CUI: C0006118
Disease: Brain Neoplasms
Brain Neoplasms
A 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011

2016

dbSNP: rs967461896
rs967461896
CUI: C0006118
Disease: Brain Neoplasms
Brain Neoplasms
G 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011

2016

dbSNP: rs967461896
rs967461896
CUI: C0006118
Disease: Brain Neoplasms
Brain Neoplasms
C 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011

2016

dbSNP: rs942158624
rs942158624
CUI: C0006118
Disease: Brain Neoplasms
Brain Neoplasms
A 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011

2016

dbSNP: rs876660821
rs876660821
CUI: C0006118
Disease: Brain Neoplasms
Brain Neoplasms
C 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011

2016

dbSNP: rs876660754
rs876660754
CUI: C0006118
Disease: Brain Neoplasms
Brain Neoplasms
A 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011

2016

dbSNP: rs876660754
rs876660754
CUI: C0006118
Disease: Brain Neoplasms
Brain Neoplasms
T 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011

2016

dbSNP: rs876659802
rs876659802
CUI: C0006118
Disease: Brain Neoplasms
Brain Neoplasms
A 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011

2016

dbSNP: rs876659675
rs876659675
CUI: C0006118
Disease: Brain Neoplasms
Brain Neoplasms
C 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011

2016

dbSNP: rs876658468
rs876658468
CUI: C0006118
Disease: Brain Neoplasms
Brain Neoplasms
T 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011

2016

dbSNP: rs876658468
rs876658468
CUI: C0006118
Disease: Brain Neoplasms
Brain Neoplasms
A 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011

2016

dbSNP: rs876658468
rs876658468
CUI: C0006118
Disease: Brain Neoplasms
Brain Neoplasms
C 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011

2016

dbSNP: rs866775781
rs866775781
CUI: C0006118
Disease: Brain Neoplasms
Brain Neoplasms
G 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011

2016

dbSNP: rs863224451
rs863224451
CUI: C0006118
Disease: Brain Neoplasms
Brain Neoplasms
A 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011

2016

dbSNP: rs863224451
rs863224451
CUI: C0006118
Disease: Brain Neoplasms
Brain Neoplasms
T 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011

2016

dbSNP: rs786203436
rs786203436
CUI: C0006118
Disease: Brain Neoplasms
Brain Neoplasms
G 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011

2016

dbSNP: rs786203436
rs786203436
CUI: C0006118
Disease: Brain Neoplasms
Brain Neoplasms
C 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011

2016

dbSNP: rs786202962
rs786202962
CUI: C0006118
Disease: Brain Neoplasms
Brain Neoplasms
A 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011

2016

dbSNP: rs786202962
rs786202962
CUI: C0006118
Disease: Brain Neoplasms
Brain Neoplasms
T 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011

2016

dbSNP: rs786201838
rs786201838
CUI: C0006118
Disease: Brain Neoplasms
Brain Neoplasms
G 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011

2016

dbSNP: rs786201838
rs786201838
CUI: C0006118
Disease: Brain Neoplasms
Brain Neoplasms
A 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011

2016