{{Rsnum
|rsid=63749810
|Chromosome=21
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=APP
|position=25891853
|Gene_s=APP
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|rsid=63749810
|Reversed=1
|FwdREF=G
|FwdALT=A
|REF=C
|ALT=T
|RSPOS=27264165
|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.27264165C>T
|CLNSRC=Neurodegenerative Brain Diseases Group; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=ADM_105; 104760.0016
|CLNSIG=5
|CLNCUI=C1854045
|CLNDBN=Cerebral amyloid angiopathy, APP-related; not provided
|Disease=Cerebral amyloid angiopathy; not provided
|CLNACC=RCV000019729.26; RCV000084564.1
|Tags=RV;PM;SLO;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet:Orphanet
|CLNDSDBID=C2751536:605714:100006:85458
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}