CCDC39, coiled-coil domain containing 39, 339829

N. diseases: 56; N. variants: 49
Disease: CILIARY DYSKINESIA, PRIMARY, 14 ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs587778820
rs587778820
Entrez Id: 339829
Gene Symbol: CCDC39
CCDC39
CUI: C3151136
Disease:
CILIARY DYSKINESIA, PRIMARY, 14 		C 0.700 CausalMutation CLINVAR