CCNO, cyclin O, 10309

N. diseases: 67; N. variants: 11
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs587777499
rs587777499
Entrez Id: 10309
Gene Symbol: CCNO
CCNO
CUI: C0008780
Disease:
Ciliary Motility Disorders 		TGGGCC 0.700 CausalMutation CLINVAR Systematic Analysis of CCNO Variants in a Defined Population: Implications for Clinical Phenotype and Differential Diagnosis. 26777464 2016
dbSNP: rs1060503388
rs1060503388
Entrez Id: 10309
Gene Symbol: CCNO
CCNO
CUI: C0008780
Disease:
Ciliary Motility Disorders 		A 0.700 CausalMutation CLINVAR Whole-Exome Sequencing and Targeted Copy Number Analysis in Primary Ciliary Dyskinesia. 26139845 2015
dbSNP: rs587777499
rs587777499
Entrez Id: 10309
Gene Symbol: CCNO
CCNO
CUI: C0008780
Disease:
Ciliary Motility Disorders 		TGGGCC 0.700 CausalMutation CLINVAR Unexpected genetic heterogeneity for primary ciliary dyskinesia in the Irish Traveller population. 24824133 2015
dbSNP: rs1060503388
rs1060503388
Entrez Id: 10309
Gene Symbol: CCNO
CCNO
CUI: C0008780
Disease:
Ciliary Motility Disorders 		A 0.700 CausalMutation CLINVAR Mutations in CCNO result in congenital mucociliary clearance disorder with reduced generation of multiple motile cilia. 24747639 2014
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
dbSNP: rs587777499
rs587777499
Entrez Id: 10309
Gene Symbol: CCNO
CCNO
CUI: C0008780
Disease:
Ciliary Motility Disorders 		TGGGCC 0.700 CausalMutation CLINVAR Mutations in CCNO result in congenital mucociliary clearance disorder with reduced generation of multiple motile cilia. 24747639 2014
dbSNP: rs587777502
rs587777502
Entrez Id: 10309
Gene Symbol: CCNO
CCNO
CUI: C0008780
Disease:
Ciliary Motility Disorders 		CGGGCT 0.700 CausalMutation CLINVAR Mutations in CCNO result in congenital mucociliary clearance disorder with reduced generation of multiple motile cilia. 24747639 2014
dbSNP: rs1554019966
rs1554019966
Entrez Id: 10309
Gene Symbol: CCNO
CCNO
CUI: C0008780
Disease:
Ciliary Motility Disorders 		C 0.700 GeneticVariation CLINVAR
dbSNP: rs587777498
rs587777498
Entrez Id: 10309
Gene Symbol: CCNO
CCNO
CUI: C4551906
Disease:
Ciliary Dyskinesia, Primary, 1, With Or Without Situs Inversus 		CGGGCA 0.700 CausalMutation CLINVAR
dbSNP: rs587777498
rs587777498
Entrez Id: 10309
Gene Symbol: CCNO
CCNO
CUI: C4014534
Disease:
CILIARY DYSKINESIA, PRIMARY, 29 		CGGGCA 0.700 CausalMutation CLINVAR
dbSNP: rs587777499
rs587777499
Entrez Id: 10309
Gene Symbol: CCNO
CCNO
CUI: C4014534
Disease:
CILIARY DYSKINESIA, PRIMARY, 29 		TGGGCC 0.700 CausalMutation CLINVAR
dbSNP: rs587777499
rs587777499
Entrez Id: 10309
Gene Symbol: CCNO
CCNO
CUI: C4551906
Disease:
Ciliary Dyskinesia, Primary, 1, With Or Without Situs Inversus 		TGGGCC 0.700 CausalMutation CLINVAR
dbSNP: rs587777500
rs587777500
Entrez Id: 10309
Gene Symbol: CCNO
CCNO
CUI: C4551906
Disease:
Ciliary Dyskinesia, Primary, 1, With Or Without Situs Inversus 		C 0.700 CausalMutation CLINVAR
dbSNP: rs587777500
rs587777500
Entrez Id: 10309
Gene Symbol: CCNO
CCNO
CUI: C4014534
Disease:
CILIARY DYSKINESIA, PRIMARY, 29 		C 0.700 CausalMutation CLINVAR
dbSNP: rs587777501
rs587777501
Entrez Id: 10309
Gene Symbol: CCNO
CCNO
CUI: C4014534
Disease:
CILIARY DYSKINESIA, PRIMARY, 29 		A 0.700 CausalMutation CLINVAR
dbSNP: rs587777501
rs587777501
Entrez Id: 10309
Gene Symbol: CCNO
CCNO
CUI: C4551906
Disease:
Ciliary Dyskinesia, Primary, 1, With Or Without Situs Inversus 		A 0.700 CausalMutation CLINVAR
dbSNP: rs587777502
rs587777502
Entrez Id: 10309
Gene Symbol: CCNO
CCNO
CUI: C4014534
Disease:
CILIARY DYSKINESIA, PRIMARY, 29 		CGGGCT 0.700 CausalMutation CLINVAR
dbSNP: rs587777502
rs587777502
Entrez Id: 10309
Gene Symbol: CCNO
CCNO
CUI: C4551906
Disease:
Ciliary Dyskinesia, Primary, 1, With Or Without Situs Inversus 		CGGGCT 0.700 CausalMutation CLINVAR
dbSNP: rs587777503
rs587777503
Entrez Id: 10309
Gene Symbol: CCNO
CCNO
CUI: C4014534
Disease:
CILIARY DYSKINESIA, PRIMARY, 29 		C 0.700 CausalMutation CLINVAR
dbSNP: rs587777503
rs587777503
Entrez Id: 10309
Gene Symbol: CCNO
CCNO
CUI: C4551906
Disease:
Ciliary Dyskinesia, Primary, 1, With Or Without Situs Inversus 		C 0.700 CausalMutation CLINVAR
dbSNP: rs774393276
rs774393276
Entrez Id: 10309
Gene Symbol: CCNO
CCNO
CUI: C0008780
Disease:
Ciliary Motility Disorders 		AC 0.700 CausalMutation CLINVAR
dbSNP: rs775051461
rs775051461
Entrez Id: 10309
Gene Symbol: CCNO
CCNO
CUI: C4014534
Disease:
CILIARY DYSKINESIA, PRIMARY, 29 		0.700 GeneticVariation UNIPROT
dbSNP: rs775051461
rs775051461
Entrez Id: 10309
Gene Symbol: CCNO
CCNO
CUI: C0008780
Disease:
Ciliary Motility Disorders 		G 0.700 CausalMutation CLINVAR
dbSNP: rs797045150
rs797045150
Entrez Id: 10309
Gene Symbol: CCNO
CCNO
CUI: C4014534
Disease:
CILIARY DYSKINESIA, PRIMARY, 29 		0.700 GeneticVariation UNIPROT
dbSNP: rs797045150
rs797045150
Entrez Id: 10309
Gene Symbol: CCNO
CCNO
CUI: C4551906
Disease:
Ciliary Dyskinesia, Primary, 1, With Or Without Situs Inversus 		C 0.700 CausalMutation CLINVAR