Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs769637393
rs769637393
Entrez Id: 8701;105375183
Gene Symbol: DNAH11;LOC105375183
DNAH11;LOC105375183
CUI: C0008780
Disease:
Ciliary Motility Disorders
T 0.700 CausalMutation CLINVAR