rs13181, KLC3;ERCC2

N. diseases: 134
Disease: Childhood Acute Myeloid Leukemia ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Childhood Acute Myeloid Leukemia
CUI: C0220621
Disease: Childhood Acute Myeloid Leukemia
0.010 GeneticVariation BEFREE We hypothesized that XPD Lys751Gln polymorphism may play a role in causation of AML in children and, as shown in adults, may affect the outcome of childhood AML therapy. 16150943 2006