{{Rsnum
|rsid=137852551
|Chromosome=X
|Orientation=minus
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene=RPGR
|position=38286070
|Gene_s=RPGR
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=312610
|variant=0022
|rsnum=137852551
}}{{ClinVar
|rsid=137852551
|Reversed=1
|FwdREF=G
|FwdALT=T
|REF=C
|ALT=A
|RSPOS=38145323
|CHROM=X
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=RPGR:6103
|GENE_NAME=RPGR
|GENE_ID=6103
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000023.10:g.38145323C>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=312610.0022
|CLNSIG=5
|CLNCUI=C1844776
|CLNDBN=Cone-rod dystrophy, X-linked 1
|Disease=Cone-rod dystrophy
|CLNACC=RCV000010596.3
|Tags=RV;PM;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C1844776:304020:1872
}}