Disease | Risk Allele | Score vda | Association Type | Original DB | Sentence supporting the association | PMID | PMID Year | ||||
---|---|---|---|---|---|---|---|---|---|---|---|
Leukemia, Myelocytic, Acute
|
0.710 | CausalMutation | CLINVAR | Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. | 26619011 | 2016 | |||||
Leukemia, Myelocytic, Acute
|
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 | |||||
Leukemia, Myelocytic, Acute
|
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 | |||||
Leukemia, Myelocytic, Acute
|
0.710 | CausalMutation | CLINVAR | The role of mutations in epigenetic regulators in myeloid malignancies. | 22898539 | 2012 | |||||
Leukemia, Myelocytic, Acute
|
0.710 | CausalMutation | CLINVAR | Cancer stem cells: Tracing clones. | 22898540 | 2012 | |||||
Leukemia, Myelocytic, Acute
|
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 | |||||
Leukemia, Myelocytic, Acute
|
0.710 | CausalMutation | CLINVAR | The role of mutations in epigenetic regulators in myeloid malignancies. | 22898539 | 2012 | |||||
Leukemia, Myelocytic, Acute
|
0.710 | CausalMutation | CLINVAR | Impact of genetic features on treatment decisions in AML. | 22160010 | 2011 | |||||
Leukemia, Myelocytic, Acute
|
0.710 | CausalMutation | CLINVAR | [Analysis of DNMT3a gene mutations in acute myelogenous leukemia]. | 21518476 | 2011 | |||||
Leukemia, Myelocytic, Acute
|
0.710 | CausalMutation | CLINVAR | [Analysis of DNMT3a gene mutations in acute myelogenous leukemia]. | 21518476 | 2011 | |||||
Leukemia, Myelocytic, Acute
|
0.710 | CausalMutation | CLINVAR | Impact of genetic features on treatment decisions in AML. | 22160010 | 2011 | |||||
Leukemia, Myelocytic, Acute
|
0.710 | CausalMutation | CLINVAR | Impact of genetic features on treatment decisions in AML. | 22160010 | 2011 | |||||
Leukemia, Myelocytic, Acute
|
0.710 | CausalMutation | CLINVAR | DNMT3A mutations in acute myeloid leukemia. | 21067377 | 2010 | |||||
Leukemia, Myelocytic, Acute
|
0.710 | CausalMutation | CLINVAR | DNMT3A mutations in acute myeloid leukemia. | 21067377 | 2010 | |||||
MYELODYSPLASTIC SYNDROME
|
0.700 | GeneticVariation | CLINVAR | Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. | 26619011 | 2016 | |||||
Adenocarcinoma of lung (disorder)
|
0.700 | GeneticVariation | CLINVAR | Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. | 26619011 | 2016 | |||||
Tatton Brown Rahman syndrome
|
0.700 | CausalMutation | CLINVAR |