DNAH11, dynein axonemal heavy chain 11, 8701

N. diseases: 110; N. variants: 109
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: rs886039340
rs886039340
Entrez Id: 8701
Gene Symbol: DNAH11
DNAH11
CUI: C0008780
Disease:
Ciliary Motility Disorders 		C 0.700 GeneticVariation CLINVAR Mutations of DNAH11 in patients with primary ciliary dyskinesia with normal ciliary ultrastructure. 22184204 2012
dbSNP: rs886039340
rs886039340
Entrez Id: 8701
Gene Symbol: DNAH11
DNAH11
CUI: C0008780
Disease:
Ciliary Motility Disorders 		C 0.700 GeneticVariation CLINVAR New DNAH11 mutations in primary ciliary dyskinesia with normal axonemal ultrastructure. 20513915 2010
dbSNP: rs886039340
rs886039340
Entrez Id: 8701
Gene Symbol: DNAH11
DNAH11
CUI: C0008780
Disease:
Ciliary Motility Disorders 		C 0.700 GeneticVariation CLINVAR Primary ciliary dyskinesia associated with normal axoneme ultrastructure is caused by DNAH11 mutations. 18022865 2008