Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs121913338
rs121913338
BRAF
0.800 GeneticVariation UNIPROT BRAF mutations in non-Hodgkin's lymphoma. 14612909

2003
dbSNP: rs121913355
rs121913355
BRAF
0.800 GeneticVariation UNIPROT BRAF mutations in non-Hodgkin's lymphoma. 14612909

2003
dbSNP: rs121913357
rs121913357
BRAF
0.800 GeneticVariation UNIPROT BRAF mutations in non-Hodgkin's lymphoma. 14612909

2003
dbSNP: rs28936699
rs28936699
CASP10
0.800 GeneticVariation UNIPROT Inactivating mutations of CASP10 gene in non-Hodgkin lymphomas. 12010812

2002
dbSNP: rs121913338
rs121913338
BRAF
C 0.800 CausalMutation CLINVAR

dbSNP: rs121913355
rs121913355
BRAF
G 0.800 CausalMutation CLINVAR

dbSNP: rs121913357
rs121913357
BRAF
G 0.800 CausalMutation CLINVAR

dbSNP: rs28936699
rs28936699
CASP10
T 0.800 CausalMutation CLINVAR

dbSNP: rs1023835002
rs1023835002
B2M ; PATL2
G 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011

2016
dbSNP: rs1023835002
rs1023835002
B2M ; PATL2
T 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011

2016
dbSNP: rs1057519877
rs1057519877
B2M ; PATL2
A 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011

2016
dbSNP: rs1057519879
rs1057519879
B2M ; PATL2
G 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011

2016
dbSNP: rs1057519879
rs1057519879
B2M ; PATL2
C 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011

2016
dbSNP: rs1057519894
rs1057519894
EZH2
G 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011

2016
dbSNP: rs1057519894
rs1057519894
EZH2
A 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011

2016
dbSNP: rs1057519909
rs1057519909
MAP2K1
C 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011

2016
dbSNP: rs1057519918
rs1057519918
MYC ; CASC11
T 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011

2016
dbSNP: rs1057519941
rs1057519941
PIK3CA
G 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011

2016
dbSNP: rs1057519941
rs1057519941
PIK3CA
C 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011

2016
dbSNP: rs1057519942
rs1057519942
PIK3CA
A 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011

2016
dbSNP: rs1057519952
rs1057519952
RHOA
A 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011

2016
dbSNP: rs1057519953
rs1057519953
RHOA
A 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011

2016
dbSNP: rs1057519953
rs1057519953
RHOA
T 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011

2016
dbSNP: rs1057519954
rs1057519954
RHOA
C 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011

2016
dbSNP: rs1057519954
rs1057519954
RHOA
A 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011

2016