{{Rsnum
|rsid=74315406
|Chromosome=20
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=PRNP
|position=4699870
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=PRNP
}}{{omim
|id=176640
|rsnum=74315406
|variant=0012
}}{{ClinVar
|rsid=74315406
|Reversed=0
|FwdREF=A
|FwdALT=G
|REF=A
|ALT=G
|RSPOS=4680516
|CHROM=20
|dbSNPBuildID=131
|SSR=0
|SAO=1
|VP=0x050368000000000002110100
|GENEINFO=PRNP:5621
|GENE_NAME=PRNP
|GENE_ID=5621
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000020.10:g.4680516A>G
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NBK1229; 176640.0012
|CLNSIG=5
|CLNCUI=C0017495; C0162534
|CLNDBN=Gerstmann-Straussler-Scheinker syndrome; Genetic prion diseases
|Disease=Gerstmann-Straussler-Scheinker syndrome; Genetic prion diseases
|CLNACC=RCV000014341.19; RCV000020256.1
|Tags=PM;PMC;S3D;SLO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:OMIM:Orphanet:SNOMED_CT; GeneReviews:MedGen
|CLNDSDBID=NBK1229:C0017495:137440:183000:356:67155006; NBK1229:C0162534
}}{{PMID Auto
|PMID=1363810
|Title=Mutant prion proteins in Gerstmann-Straussler-Scheinker disease with neurofibrillary tangles.
}}