{{Rsnum
|rsid=387906971
|Chromosome=17
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=PRPF8
|position=1653558
|Gene_s=PRPF8
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=A
|CHROM=17
|CLNACC=RCV000023643.1
|CLNALLE=1
|CLNDBN=Retinitis pigmentosa 13
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1417:C1838702:600059:791
|CLNHGVS=NC_000017.10:g.1556852G>A
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=607300.0006
|Disease=Retinitis pigmentosa 13
|FwdALT=T
|FwdREF=C
|REF=G
|RSPOS=1556852
|Reversed=1
|SAO=0
|SSR=0
|Tags=RV;PM;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050060000000000002110100
|WGT=0
|dbSNPBuildID=137
|rsid=387906971
|GENEINFO=PRPF8:10594
|GENE_ID=10594
|GENE_NAME=PRPF8
}}