Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs879255568
rs879255568
Entrez Id: 23568
Gene Symbol: ARL2BP
ARL2BP
CUI: C0035334
Disease:
Retinitis Pigmentosa
C 0.700 CausalMutation CLINVAR