Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs137853290
rs137853290
Entrez Id: 6017
Gene Symbol: RLBP1
RLBP1
CUI: C4551633
Disease:
Pigmentary retinal dystrophy
0.010 GeneticVariation BEFREE Fundus albipunctatus and retinitis punctata albescens in a pedigree with an R150Q mutation in RLBP1. 11453974 2001