{{Rsnum
|rsid = 29001566
|Gene = RHO
|Orientation=plus
|ReferenceAllele=C
|MissenseAllele=T
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Chromosome=3
|position=129533711
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=RHO
}}{{omim
|desc=RETINITIS PIGMENTOSA 4
|id=180380
|rsnum=29001566
|variant=0020
}}
{{ neighbor
| rsid = 29001637
| distance = 1
}}
{{omim
|id=180380
|rsnum=29001566
|variant=0002
}}
{{omim
|id=180380
|rsnum=29001566
|variant=0041
}}{{ClinVar
|rsid=29001566
|Reversed=0
|FwdREF=C
|FwdALT=A,G,T
|REF=C
|ALT=A,G,T
|RSPOS=129252554
|CHROM=3
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050260000000000002110104
|GENEINFO=RHO:6010
|GENE_NAME=RHO
|GENE_ID=6010
|WGT=0
|VC=SNV
|CLNALLE=1; 2; 3
|CLNHGVS=NC_000003.11:g.129252554C>A; NC_000003.11:g.129252554C>G; NC_000003.11:g.129252554C>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=180380.0041; 180380.0020; 180380.0002
|CLNSIG=5
|CLNCUI=C1867176
|CLNDBN=Retinitis pigmentosa 4
|Disease=Retinitis pigmentosa 4
|CLNACC=RCV000013928.22; RCV000013907.22; RCV000013888.16
|Tags=PM;S3D;OTHERKG;LSD;OM;NOV
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1417:C3151001:613731:791
}}