{{Rsnum
|rsid=104893779
|Chromosome=3
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=RHO
|position=129532288
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=RHO
}}{{omim
|id=180380
|rsnum=104893779
|variant=0027
}}
{{omim
|id=180380
|rsnum=104893779
|variant=0017
}}{{ClinVar
|rsid=104893779
|Reversed=0
|FwdREF=G
|FwdALT=A,T
|REF=G
|ALT=A,T
|RSPOS=129251131
|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; 2
|CLNHGVS=NC_000003.11:g.129251131G>A; NC_000003.11:g.129251131G>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=180380.0017; 180380.0027
|CLNSIG=5
|CLNCUI=C1867176
|CLNDBN=Retinitis pigmentosa 4
|Disease=Retinitis pigmentosa 4
|CLNACC=RCV000013897.23; RCV000013915.16
|Tags=PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1417:C3151001:613731:791
}}