{{Rsnum
|rsid=63750579
|Chromosome=21
|Orientation=minus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=APP
|position=25891856
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=APP
}}{{omim
|id=104760
|rsnum=63750579
|variant=0001
}}
{{omim
|id=104760
|rsnum=63750579
|variant=0014
}}{{ClinVar
|rsid=63750579
|Reversed=1
|FwdREF=G
|FwdALT=A,C
|REF=C
|ALT=G,T
|RSPOS=27264168
|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; 2
|CLNHGVS=NC_000021.8:g.27264168C>G; NC_000021.8:g.27264168C>T
|CLNSRC=OMIM Allelic Variant; Neurodegenerative Brain Diseases Group
|CLNORIGIN=1
|CLNSRCID=104760.0001; ADM_153; 104760.0014
|CLNSIG=5
|CLNCUI=C1854045
|CLNDBN=Cerebral amyloid angiopathy, APP-related; not provided
|Disease=Cerebral amyloid angiopathy; not provided
|CLNACC=RCV000019713.26; RCV000019727.26; RCV000084562.1
|Tags=RV;PM;SLO;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet:Orphanet
|CLNDSDBID=C2751536:605714:100006:85458
}}