Source: CLINVAR

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
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

dbSNP: rs786201838
rs786201838
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: rs786201059
rs786201059
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: rs786201059
rs786201059
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: rs786201057
rs786201057
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: rs786201057
rs786201057
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: rs769696078
rs769696078
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: rs765848205
rs765848205
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: rs760043106
rs760043106
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: rs760043106
rs760043106
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: rs753660142
rs753660142
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: rs747342068
rs747342068
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: rs747342068
rs747342068
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: rs730882026
rs730882026
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: rs730882025
rs730882025
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: rs730882025
rs730882025
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: rs730882008
rs730882008
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: rs730882008
rs730882008
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: rs730882005
rs730882005
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: rs730882005
rs730882005
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