Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs746242380
rs746242380
Entrez Id: 388389;100528020
Gene Symbol: CCDC103;FAM187A
CCDC103;FAM187A
CUI: C0008780
Disease:
Ciliary Motility Disorders
CAG 0.700 CausalMutation CLINVAR
dbSNP: rs746242380
rs746242380
Entrez Id: 388389;100528020
Gene Symbol: CCDC103;FAM187A
CCDC103;FAM187A
CUI: C0008780
Disease:
Ciliary Motility Disorders
CAG 0.700 GeneticVariation CLINVAR