{{Rsnum
|rsid=104894927
|Chromosome=X
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=RP2
|position=46853731
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=RP2
}}{{omim
|id=300757
|rsnum=104894927
|variant=0008
}}{{ClinVar
|rsid=104894927
|Reversed=0
|FwdREF=C
|FwdALT=T
|REF=C
|ALT=T
|RSPOS=46713166
|CHROM=X
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=RP2:6102
|GENE_NAME=RP2
|GENE_ID=6102
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000023.10:g.46713166C>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=300757.0008
|CLNSIG=5
|CLNCUI=C2681923
|CLNDBN=Retinitis pigmentosa 2
|Disease=Retinitis pigmentosa 2
|CLNACC=RCV000011297.3
|Tags=PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1417:C2681923:312600:791
}}