CCNO, cyclin O, 10309

N. diseases: 67; N. variants: 11
Disease: Ciliary Motility Disorders ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs587777498
rs587777498
Entrez Id: 10309
Gene Symbol: CCNO
CCNO
CUI: C0008780
Disease:
Ciliary Motility Disorders 		CGGGCA 0.700 CausalMutation CLINVAR Mutations in CCNO result in congenital mucociliary clearance disorder with reduced generation of multiple motile cilia. 24747639 2014