{{Rsnum
|rsid=63750921
|Chromosome=21
|Orientation=minus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=APP
|position=25891820
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=APP
}}{{omim
|id=104760
|rsnum=63750921
|variant=0019
}}{{ClinVar
|rsid=63750921
|Reversed=1
|FwdREF=C
|FwdALT=G
|REF=G
|ALT=C
|RSPOS=27264132
|CHROM=21
|dbSNPBuildID=136
|SSR=0
|SAO=1
|VP=0x050160000000000002110100
|GENEINFO=APP:351
|GENE_NAME=APP
|GENE_ID=351
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000021.8:g.27264132G>C
|CLNORIGIN=1
|CLNSIG=5
|Tags=RV;PM;SLO;OTHERKG;LSD;OM
|CLNACC=RCV000019731.25; RCV000084565.1
|CLNDBN=CEREBRAL AMYLOID ANGIOPATHY, APP-RELATED, PIEDMONT VARIANT; not provided
|CLNSRC=Neurodegenerative Brain Diseases Group; OMIM Allelic Variant
|CLNSRCID=ADM_247; 104760.0019
|Disease=CEREBRAL AMYLOID ANGIOPATHY; not provided
}}