Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs267606870
rs267606870
IDH2
A 0.710 CausalMutation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011

2016
dbSNP: rs267606870
rs267606870
IDH2
A 0.710 CausalMutation CLINVAR Prognostic relevance of integrated genetic profiling in acute myeloid leukemia. 22417203

2012
dbSNP: rs267606870
rs267606870
IDH2
A 0.710 CausalMutation CLINVAR The role of mutations in epigenetic regulators in myeloid malignancies. 22898539

2012
dbSNP: rs267606870
rs267606870
IDH2
A 0.710 CausalMutation CLINVAR Impact of genetic features on treatment decisions in AML. 22160010

2011
dbSNP: rs267606870
rs267606870
IDH2
0.710 GeneticVariation BEFREE IDH2 mutations included R140Q (n=3; one post-PMF AML, one post-PV AML and one PMF) and a novel R140W (n=1; mutation found in both chronic- and blast-phase samples). 20410924

2010