Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs104894187
rs104894187
Entrez Id: 5995
Gene Symbol: RGR
RGR
CUI: C3151068
Disease:
RETINITIS PIGMENTOSA 44
0.700 GeneticVariation UNIPROT Mutations in RGR, encoding a light-sensitive opsin homologue, in patients with retinitis pigmentosa. 10581022 1999