{{Rsnum
|rsid=104893796
|Chromosome=3
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=RHO
|position=129529014
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=RHO
}}{{omim
|id=180380
|rsnum=104893796
|variant=0042
}}{{ClinVar
|rsid=104893796
|Reversed=0
|FwdREF=C
|FwdALT=T
|REF=C
|ALT=T
|RSPOS=129247857
|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.129247857C>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=180380.0042
|CLNSIG=5
|CLNCUI=C1864869
|CLNDBN=Congenital stationary night blindness, autosomal dominant 1
|Disease=Congenital stationary night blindness
|CLNACC=RCV000013929.23
|Tags=PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C1864869:610445:215
}}