{{Rsnum
|rsid=104893775
|Chromosome=3
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=RHO
|position=129530917
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=RHO
}}{{omim
|id=180380
|rsnum=104893775
|variant=0012
}}{{ClinVar
|rsid=104893775
|Reversed=0
|FwdREF=C
|FwdALT=T
|REF=C
|ALT=T
|RSPOS=129249760
|CHROM=3
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=RHO:6010
|GENE_NAME=RHO
|GENE_ID=6010
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000003.11:g.129249760C>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=180380.0012
|CLNSIG=5
|CLNCUI=C1867176
|CLNDBN=Retinitis pigmentosa 4; Retinitis punctata albescens
|Disease=Retinitis pigmentosa 4; Retinitis punctata albescens
|CLNACC=RCV000013902.23; RCV000013903.23
|Tags=PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet; MedGen
|CLNDSDBID=NBK1417:C3151001:613731:791; C1405854
}}