{{Rsnum
|rsid=74315408
|Gene=PRNP
|Chromosome=20
|position=4699758
|Orientation=plus
|GMAF=0.0004591
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=PRNP
}}{{omim
|id=176640
|rsnum=74315408
|variant=0016
}}{{ClinVar
|rsid=74315408
|Reversed=0
|FwdREF=G
|FwdALT=A
|REF=G
|ALT=A
|RSPOS=4680404
|CHROM=20
|GMAF=0.0005
|dbSNPBuildID=131
|SSR=0
|SAO=1
|VP=0x050368000000000016110100
|GENEINFO=PRNP:5621
|GENE_NAME=PRNP
|GENE_ID=5621
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000020.10:g.4680404G>A
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NBK1229; 176640.0016
|CLNSIG=5
|CLNCUI=C0022336; C0162534
|CLNDBN=Jakob-Creutzfeldt disease; Genetic prion diseases
|Disease=Jakob-Creutzfeldt disease; Genetic prion diseases
|CLNACC=RCV000014344.23; RCV000020249.1
|Tags=PM;PMC;S3D;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.
}}

{{PMID Auto
|PMID=14872044
|Title=Clinical features of Creutzfeldt-Jakob disease with V180I mutation.
}}