{{Rsnum
|rsid=80356711
|Chromosome=20
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=PRNP
|position=4699698
|Gene_s=PRNP
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|rsid=80356711
|Reversed=0
|FwdREF=C
|FwdALT=T
|REF=C
|ALT=T
|RSPOS=4680344
|CHROM=20
|dbSNPBuildID=131
|SSR=0
|SAO=1
|VP=0x050360000000000002110100
|GENEINFO=PRNP:5621
|GENE_NAME=PRNP
|GENE_ID=5621
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000020.10:g.4680344C>T
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNORIGIN=0
|CLNSRCID=NBK1229; 176640.0032
|CLNSIG=5
|CLNCUI=C0162534
|CLNDBN=Genetic prion diseases; CEREBRAL AMYLOID ANGIOPATHY, PRNP-RELATED
|Disease=Genetic prion diseases; CEREBRAL AMYLOID ANGIOPATHY
|CLNACC=RCV000020246.1; RCV000074470.13
|Tags=PM;S3D;SLO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen; MedGen
|CLNDSDBID=NBK1229:C0162534; CN181778
}}