DDX58, DExD/H-box helicase 58, 23586

N. diseases: 144; N. variants: 10
Disease: SINGLETON-MERTEN SYNDROME 2 ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs786204847
rs786204847
Entrez Id: 23586
Gene Symbol: DDX58
DDX58
CUI: C4225380
Disease:
SINGLETON-MERTEN SYNDROME 2 		G 0.800 CausalMutation CLINVAR
dbSNP: rs786204847
rs786204847
Entrez Id: 23586
Gene Symbol: DDX58
DDX58
CUI: C4225380
Disease:
SINGLETON-MERTEN SYNDROME 2 		0.800 GeneticVariation UNIPROT