DDX41, DEAD-box helicase 41, 51428

N. diseases: 54; N. variants: 10
Disease: MYELOPROLIFERATIVE/LYMPHOPROLIFERATIVE NEOPLASMS, FAMILIAL (MULTIPLE TYPES), SUSCEPTIBILITY TO ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs141601766
rs141601766
Entrez Id: 51428
Gene Symbol: DDX41
DDX41
CUI: C4225174
Disease:
MYELOPROLIFERATIVE/LYMPHOPROLIFERATIVE NEOPLASMS, FAMILIAL (MULTIPLE TYPES), SUSCEPTIBILITY TO 		T 0.700 CausalMutation CLINVAR
dbSNP: rs141601766
rs141601766
Entrez Id: 51428
Gene Symbol: DDX41
DDX41
CUI: C4225174
Disease:
MYELOPROLIFERATIVE/LYMPHOPROLIFERATIVE NEOPLASMS, FAMILIAL (MULTIPLE TYPES), SUSCEPTIBILITY TO 		T 0.700 SusceptibilityMutation CLINVAR