{{Rsnum
|rsid=387907268
|Chromosome=17
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=PRCD
|position=76540205
|Gene_s=PRCD
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=T
|CHROM=17
|CLNACC=RCV000030701.1
|CLNALLE=1
|CLNDBN=Retinitis pigmentosa 36
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1417:C1864621:610599:791
|CLNHGVS=NC_000017.10:g.74536287C>T
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=610598.0002
|Disease=Retinitis pigmentosa 36
|FwdALT=T
|FwdREF=C
|REF=C
|RSPOS=74536287
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050060000000000002110100
|WGT=0
|dbSNPBuildID=137
|rsid=387907268
|GENEINFO=PRCD:768206
|GENE_ID=768206
|GENE_NAME=PRCD
}}