Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1554824273
rs1554824273
Entrez Id: 5995
Gene Symbol: RGR
RGR
CUI: C0854723
Disease:
Retinal Dystrophies
AG 0.700 CausalMutation CLINVAR Mutations in RGR, encoding a light-sensitive opsin homologue, in patients with retinitis pigmentosa. 10581022 1999