RBP3, retinol binding protein 3, 5949

N. diseases: 73; N. variants: 5
Disease: Night blindness, congenital stationary ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs782604129
rs782604129
Entrez Id: 5949
Gene Symbol: RBP3
RBP3
CUI: C0339535
Disease:
Night blindness, congenital stationary 		A 0.700 GeneticVariation CLINVAR