Source: CLINVAR

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs746242380
rs746242380
CCDC103 ; FAM187A
CUI: C0008780
Disease: Ciliary Motility Disorders
Ciliary Motility Disorders 		CAG 0.700 CausalMutation CLINVAR

dbSNP: rs746242380
rs746242380
CCDC103 ; FAM187A
CUI: C0008780
Disease: Ciliary Motility Disorders
Ciliary Motility Disorders 		CAG 0.700 GeneticVariation CLINVAR