{{Rsnum
|rsid=74315409
|Gene=PRNP
|Chromosome=20
|position=4699915
|Orientation=plus
|GMAF=0.0004591
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene_s=PRNP
}}{{omim
|id=176640
|rsnum=74315409
|variant=0017
}}{{ClinVar
|rsid=74315409
|Reversed=0
|FwdREF=T
|FwdALT=G
|REF=T
|ALT=G
|RSPOS=4680561
|CHROM=20
|GMAF=0.0005
|dbSNPBuildID=131
|SSR=0
|SAO=1
|VP=0x050168000000000016110100
|GENEINFO=PRNP:5621
|GENE_NAME=PRNP
|GENE_ID=5621
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000020.10:g.4680561T>G
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNORIGIN=0
|CLNSRCID=NBK1229; 176640.0017
|CLNSIG=5
|CLNCUI=C0022336; C0752347; C0162534
|CLNDBN=Jakob-Creutzfeldt disease; Genetic prion diseases
|Disease=Jakob-Creutzfeldt disease; Genetic prion diseases
|CLNACC=RCV000014345.11; RCV000020258.1
|Tags=PM;PMC;SLO;KGPhase1;KGPROD;OTHERKG;LSD;OM
|CAF=0.9995; 0.0004591
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT; GeneReviews:MedGen
|CLNDSDBID=NBK1229:C0022336:123400:204:792004; NBK1229:C0162534
|COMMON=0
}}{{PMID Auto
|PMID=8461023
|Title=Novel missense variants of prion protein in Creutzfeldt-Jakob disease or Gerstmann-Straussler syndrome.
}}