Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1285431486
rs1285431486
Entrez Id: 339829
Gene Symbol: CCDC39
CCDC39
CUI: C0008780
Disease:
Ciliary Motility Disorders
T 0.700 CausalMutation CLINVAR