DDX41, DEAD-box helicase 41, 51428

N. diseases: 54; N. variants: 10
Disease: Childhood Myelodysplastic Syndrome ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs869312828
rs869312828
Entrez Id: 51428;79930
Gene Symbol: DDX41;DOK3
DDX41;DOK3
CUI: C2347761
Disease:
Childhood Myelodysplastic Syndrome 		0.010 GeneticVariation BEFREE The R525H mutation in DDX41 is thought to play important roles in the development of hereditary myelodysplastic syndrome and acute myelocytic leukemia. 28426938 2017