Variant | Gene | Risk Allele | Score vda | Association Type | Original DB | Sentence supporting the association | PMID | PMID Year | ||
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G | 0.700 | GeneticVariation | CLINVAR | RUNX1 mutation associated with clonal evolution in relapsed pediatric acute myeloid leukemia with t(16;21)(p11;q22). | 24374719 | 2014 |
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G | 0.700 | GeneticVariation | CLINVAR | Clinical impact of gene mutations and lesions detected by SNP-array karyotyping in acute myeloid leukemia patients in the context of gemtuzumab ozogamicin treatment: results of the ALFA-0701 trial. | 24659740 | 2014 |
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A | 0.700 | GeneticVariation | CLINVAR | Minimal residual disease monitoring in t(8;21) acute myeloid leukemia based on RUNX1-RUNX1T1 fusion quantification on genomic DNA. | 24616160 | 2014 |
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G | 0.700 | GeneticVariation | CLINVAR | Minimal residual disease monitoring in t(8;21) acute myeloid leukemia based on RUNX1-RUNX1T1 fusion quantification on genomic DNA. | 24616160 | 2014 |
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|
A | 0.700 | GeneticVariation | CLINVAR | RUNX1 mutation associated with clonal evolution in relapsed pediatric acute myeloid leukemia with t(16;21)(p11;q22). | 24374719 | 2014 |
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|
A | 0.700 | GeneticVariation | CLINVAR | Clinical impact of gene mutations and lesions detected by SNP-array karyotyping in acute myeloid leukemia patients in the context of gemtuzumab ozogamicin treatment: results of the ALFA-0701 trial. | 24659740 | 2014 |
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|
T | 0.700 | GeneticVariation | CLINVAR | Clinical impact of gene mutations and lesions detected by SNP-array karyotyping in acute myeloid leukemia patients in the context of gemtuzumab ozogamicin treatment: results of the ALFA-0701 trial. | 24659740 | 2014 |
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|
T | 0.700 | GeneticVariation | CLINVAR | High frequency of RUNX1 biallelic alteration in acute myeloid leukemia secondary to familial platelet disorder. | 19357396 | 2009 |
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A | 0.700 | GeneticVariation | CLINVAR | Haploinsufficiency of CBFA2 causes familial thrombocytopenia with propensity to develop acute myelogenous leukaemia. | 10508512 | 1999 |