Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs782469310
rs782469310
Entrez Id: 5949
Gene Symbol: RBP3
RBP3
CUI: C0854723
Disease:
Retinal Dystrophies
T 0.700 GeneticVariation CLINVAR Whole Genome Sequencing Increases Molecular Diagnostic Yield Compared with Current Diagnostic Testing for Inherited Retinal Disease. 26872967 2016