Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs121913232
rs121913232
C 0.710 CausalMutation CLINVAR Prospective enterprise-level molecular genotyping of a cohort of cancer patients. 25157968

2014

dbSNP: rs121913232
rs121913232
C 0.710 CausalMutation CLINVAR The role of kinase inhibitors in the treatment of patients with acute myeloid leukemia. 23714533

2013

dbSNP: rs121913232
rs121913232
C 0.710 CausalMutation CLINVAR Mutational landscape of AML with normal cytogenetics: biological and clinical implications. 23261068

2013

dbSNP: rs121913232
rs121913232
C 0.710 CausalMutation CLINVAR Prospective evaluation of gene mutations and minimal residual disease in patients with core binding factor acute myeloid leukemia. 23321257

2013

dbSNP: rs121913232
rs121913232
C 0.710 CausalMutation CLINVAR The importance of relative mutant level for evaluating impact on outcome of KIT, FLT3 and CBL mutations in core-binding factor acute myeloid leukemia. 23783394

2013

dbSNP: rs121913232
rs121913232
C 0.710 CausalMutation CLINVAR Continuing aspirin in the perioperative patient. 22504186

2012

dbSNP: rs121913232
rs121913232
C 0.710 CausalMutation CLINVAR Sorafenib treatment of FLT3-ITD(+) acute myeloid leukemia: favorable initial outcome and mechanisms of subsequent nonresponsiveness associated with the emergence of a D835 mutation. 22368270

2012

dbSNP: rs121913232
rs121913232
C 0.710 CausalMutation CLINVAR [FMS-like tyrosine kinase 3 gene mutations in acute myeloid leukemia]. 19840437

2009

dbSNP: rs121913232
rs121913232
0.710 GeneticVariation BEFREE Recently, novel mutations within the activation loop were identified in patients with AML: deletion of isoleucine 836 (Ile836del) and an exchange of isoleucine 836 to methionine plus an arginine insertion (Ile836Met+Arg). 12663439

2003