{{Rsnum
|rsid=146150511
|Chromosome=10
|position=47353508
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=RBP3
|Gene_s=RBP3
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=T
|CHROM=10
|CLNACC=RCV000043517.17
|CLNALLE=1
|CLNDBN=Retinitis pigmentosa 66
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=CN169677:615233:791
|CLNHGVS=NC_000010.10:g.48385854C>T
|CLNORIGIN=1
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=180290.0001
|Disease=Retinitis pigmentosa 66
|FwdALT=T
|FwdREF=C
|GENEINFO=RBP3:5949
|GENE_ID=5949
|GENE_NAME=RBP3
|REF=C
|RSPOS=48385854
|Reversed=0
|SAO=1
|SSR=0
|Tags=PM;PMC;S3D;OTHERKG;LSD
|VC=SNV
|VP=0x050268000000000002100100
|WGT=0
|dbSNPBuildID=134
|rsid=146150511
}}{{PMID Auto
|PMID=19074801
|Title=A homozygous missense mutation in the IRBP gene (RBP3) associated with autosomal recessive retinitis pigmentosa.
|OA=1
}}