{{Rsnum
|rsid=121434241
|Chromosome=1
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=PRPF3
|position=150344216
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=PRPF3
}}{{omim
|id=607301
|rsnum=121434241
|variant=0001
}}{{ClinVar
|rsid=121434241
|Reversed=0
|FwdREF=C
|FwdALT=T
|REF=C
|ALT=T
|RSPOS=150344216
|CHROM=1
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050060000a05000002110100
|GENEINFO=PRPF3:9129
|GENE_NAME=PRPF3
|GENE_ID=9129
|WGT=1
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000001.11:g.150344216C>T
|CLNSRC=ClinVar; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NM_004698.2:c.1481C>T; 607301.0001
|CLNSIG=5
|CLNCUI=C1832378
|CLNDBN=Retinitis pigmentosa 18
|Disease=Retinitis pigmentosa 18
|CLNACC=RCV000003516.1
|Tags=PM;NSM;REF;ASP;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1417:C1832378:601414:ORPHA791
}}