Gene: KRAS ×
Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs121913529
rs121913529
KRAS
0.710 GeneticVariation BEFREE KRAS (G12D) cooperates with AML1/ETO to initiate a mouse model mimicking human acute myeloid leukemia. 24480914

2014
dbSNP: rs121913529
rs121913529
KRAS
A 0.710 GeneticVariation CLINVAR RAS mutations are frequent in FAB type M4 and M5 of acute myeloid leukemia, and related to late relapse: a study of the Japanese Childhood AML Cooperative Study Group. 22407852

2012
dbSNP: rs121913529
rs121913529
KRAS
T 0.710 GeneticVariation CLINVAR RAS mutations are frequent in FAB type M4 and M5 of acute myeloid leukemia, and related to late relapse: a study of the Japanese Childhood AML Cooperative Study Group. 22407852

2012
dbSNP: rs121913529
rs121913529
KRAS
T 0.710 GeneticVariation CLINVAR High-throughput sequencing screen reveals novel, transforming RAS mutations in myeloid leukemia patients. 19075190

2009
dbSNP: rs121913529
rs121913529
KRAS
A 0.710 GeneticVariation CLINVAR High-throughput sequencing screen reveals novel, transforming RAS mutations in myeloid leukemia patients. 19075190

2009
dbSNP: rs121913529
rs121913529
KRAS
A 0.710 GeneticVariation CLINVAR Implications of NRAS mutations in AML: a study of 2502 patients. 16434492

2006
dbSNP: rs121913529
rs121913529
KRAS
T 0.710 GeneticVariation CLINVAR Implications of NRAS mutations in AML: a study of 2502 patients. 16434492

2006
dbSNP: rs121913529
rs121913529
KRAS
T 0.710 GeneticVariation CLINVAR RAS gene mutations in childhood acute myeloid leukemia: a Pediatric Oncology Group study. 2278970

1990
dbSNP: rs121913529
rs121913529
KRAS
A 0.710 GeneticVariation CLINVAR RAS gene mutations in childhood acute myeloid leukemia: a Pediatric Oncology Group study. 2278970

1990
dbSNP: rs121913529
rs121913529
KRAS
A 0.710 GeneticVariation CLINVAR RAS gene mutations in acute and chronic myelocytic leukemias, chronic myeloproliferative disorders, and myelodysplastic syndromes. 3122217

1987
dbSNP: rs121913529
rs121913529
KRAS
T 0.710 GeneticVariation CLINVAR RAS gene mutations in acute and chronic myelocytic leukemias, chronic myeloproliferative disorders, and myelodysplastic syndromes. 3122217

1987
dbSNP: rs17851045
rs17851045
KRAS
A 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011

2016
dbSNP: rs104894366
rs104894366
KRAS
C 0.700 CausalMutation CLINVAR Structure-energy-based predictions and network modelling of RASopathy and cancer missense mutations. 24803665

2014
dbSNP: rs112445441
rs112445441
KRAS
T 0.700 GeneticVariation CLINVAR RAS mutations are frequent in FAB type M4 and M5 of acute myeloid leukemia, and related to late relapse: a study of the Japanese Childhood AML Cooperative Study Group. 22407852

2012
dbSNP: rs17851045
rs17851045
KRAS
A 0.700 GeneticVariation CLINVAR RAS mutations are frequent in FAB type M4 and M5 of acute myeloid leukemia, and related to late relapse: a study of the Japanese Childhood AML Cooperative Study Group. 22407852

2012
dbSNP: rs17851045
rs17851045
KRAS
G 0.700 GeneticVariation CLINVAR RAS mutations are frequent in FAB type M4 and M5 of acute myeloid leukemia, and related to late relapse: a study of the Japanese Childhood AML Cooperative Study Group. 22407852

2012
dbSNP: rs104894366
rs104894366
KRAS
C 0.700 CausalMutation CLINVAR Germline KRAS mutations cause aberrant biochemical and physical properties leading to developmental disorders. 20949621

2011
dbSNP: rs112445441
rs112445441
KRAS
T 0.700 GeneticVariation CLINVAR High-throughput sequencing screen reveals novel, transforming RAS mutations in myeloid leukemia patients. 19075190

2009
dbSNP: rs17851045
rs17851045
KRAS
G 0.700 GeneticVariation CLINVAR High-throughput sequencing screen reveals novel, transforming RAS mutations in myeloid leukemia patients. 19075190

2009
dbSNP: rs17851045
rs17851045
KRAS
A 0.700 GeneticVariation CLINVAR High-throughput sequencing screen reveals novel, transforming RAS mutations in myeloid leukemia patients. 19075190

2009
dbSNP: rs104894366
rs104894366
KRAS
C 0.700 CausalMutation CLINVAR Germline KRAS mutations cause Noonan syndrome. 16474405

2006
dbSNP: rs112445441
rs112445441
KRAS
T 0.700 GeneticVariation CLINVAR Implications of NRAS mutations in AML: a study of 2502 patients. 16434492

2006
dbSNP: rs17851045
rs17851045
KRAS
A 0.700 GeneticVariation CLINVAR Implications of NRAS mutations in AML: a study of 2502 patients. 16434492

2006
dbSNP: rs17851045
rs17851045
KRAS
G 0.700 GeneticVariation CLINVAR Implications of NRAS mutations in AML: a study of 2502 patients. 16434492

2006
dbSNP: rs112445441
rs112445441
KRAS
T 0.700 GeneticVariation CLINVAR RAS gene mutations in childhood acute myeloid leukemia: a Pediatric Oncology Group study. 2278970

1990