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: rs1060503433
rs1060503433
Entrez Id: 9343;388389;100528020
Gene Symbol: EFTUD2;CCDC103;FAM187A
EFTUD2;CCDC103;FAM187A
CUI: C0008780
Disease:
Ciliary Motility Disorders 		T 0.700 CausalMutation CLINVAR