Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs147001633
rs147001633
G 0.800 CausalMutation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011

2016

dbSNP: rs147001633
rs147001633
T 0.800 CausalMutation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011

2016

dbSNP: rs147001633
rs147001633
T 0.800 CausalMutation CLINVAR AML cells with the R882H mutation have severely reduced de novo methyltransferase activity and focal hypomethylation at specific CpGs throughout AML cell genomes. 24656771

2014

dbSNP: rs147001633
rs147001633
T 0.800 CausalMutation CLINVAR Molecular evaluation of DNMT3A and IDH1/2 gene mutation: frequency, distribution pattern and associations with additional molecular markers in normal karyotype Indian acute myeloid leukemia patients. 24606448

2014

dbSNP: rs147001633
rs147001633
A 0.800 CausalMutation CLINVAR Cancer stem cells: Tracing clones. 22898540

2012

dbSNP: rs147001633
rs147001633
G 0.800 CausalMutation CLINVAR Retroviral oncogenes: a historical primer. 22898541

2012

dbSNP: rs147001633
rs147001633
T 0.800 CausalMutation CLINVAR The role of mutations in epigenetic regulators in myeloid malignancies. 22898539

2012

dbSNP: rs147001633
rs147001633
T 0.800 CausalMutation CLINVAR Three heterozygous mutations (p.R882S, p.R882C and p.R882H) were identified in three of 61 AML patients, whereas none of patients with other hematological disorders harbored any mutation. 22744846

2012

dbSNP: rs147001633
rs147001633
A 0.800 CausalMutation CLINVAR Impact of genetic features on treatment decisions in AML. 22160010

2011

dbSNP: rs147001633
rs147001633
T 0.800 CausalMutation CLINVAR Impact of genetic features on treatment decisions in AML. 22160010

2011

dbSNP: rs147001633
rs147001633
T 0.800 CausalMutation CLINVAR [Analysis of DNMT3a gene mutations in acute myelogenous leukemia]. 21518476

2011

dbSNP: rs147001633
rs147001633
G 0.800 CausalMutation CLINVAR Impact of genetic features on treatment decisions in AML. 22160010

2011

dbSNP: rs147001633
rs147001633
T 0.800 CausalMutation CLINVAR DNMT3A mutations in acute myeloid leukemia. 21067377

2010

dbSNP: rs147001633
rs147001633
G 0.800 CausalMutation CLINVAR DNMT3A mutations in acute myeloid leukemia. 21067377

2010

dbSNP: rs377577594
rs377577594
A 0.710 CausalMutation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011

2016

dbSNP: rs377577594
rs377577594
A 0.710 CausalMutation CLINVAR Molecular evaluation of DNMT3A and IDH1/2 gene mutation: frequency, distribution pattern and associations with additional molecular markers in normal karyotype Indian acute myeloid leukemia patients. 24606448

2014

dbSNP: rs377577594
rs377577594
A 0.710 CausalMutation CLINVAR Three heterozygous mutations (p.R882S, p.R882C and p.R882H) were identified in three of 61 AML patients, whereas none of patients with other hematological disorders harbored any mutation. 22744846

2012

dbSNP: rs377577594
rs377577594
C 0.710 CausalMutation CLINVAR The role of mutations in epigenetic regulators in myeloid malignancies. 22898539

2012

dbSNP: rs377577594
rs377577594
T 0.710 CausalMutation CLINVAR Cancer stem cells: Tracing clones. 22898540

2012

dbSNP: rs377577594
rs377577594
T 0.710 CausalMutation CLINVAR Three heterozygous mutations (p.R882S, p.R882C and p.R882H) were identified in three of 61 AML patients, whereas none of patients with other hematological disorders harbored any mutation. 22744846

2012

dbSNP: rs377577594
rs377577594
A 0.710 CausalMutation CLINVAR The role of mutations in epigenetic regulators in myeloid malignancies. 22898539

2012

dbSNP: rs377577594
rs377577594
T 0.710 CausalMutation CLINVAR Impact of genetic features on treatment decisions in AML. 22160010

2011

dbSNP: rs377577594
rs377577594
T 0.710 CausalMutation CLINVAR [Analysis of DNMT3a gene mutations in acute myelogenous leukemia]. 21518476

2011

dbSNP: rs377577594
rs377577594
A 0.710 CausalMutation CLINVAR [Analysis of DNMT3a gene mutations in acute myelogenous leukemia]. 21518476

2011

dbSNP: rs377577594
rs377577594
A 0.710 CausalMutation CLINVAR Impact of genetic features on treatment decisions in AML. 22160010

2011