{{Rsnum
|rsid=63751399
|Chromosome=14
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=PSEN1
|position=73171047
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=PSEN1
}}{{omim
|id=104311
|rsnum=63751399
|variant=0023
}}{{ClinVar
|rsid=63751399
|Reversed=0
|FwdREF=T
|FwdALT=C
|REF=T
|ALT=C
|RSPOS=73637755
|CHROM=14
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050168000000000002110100
|GENEINFO=PSEN1:5663
|GENE_NAME=PSEN1
|GENE_ID=5663
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000014.8:g.73637755T>C
|CLNSRC=GeneReviews; Neurodegenerative Brain Diseases Group; OMIM Allelic Variant
|CLNORIGIN=0
|CLNSRCID=NBK1236; ADM_102; 104311.0023
|CLNSIG=5
|CLNCUI=C0338451; C1843013
|CLNDBN=Frontotemporal dementia; Alzheimer disease, type 3; not provided
|Disease=Frontotemporal dementia; Alzheimer disease; not provided
|CLNACC=RCV000019775.26; RCV000020084.1; RCV000084292.1
|Tags=PM;PMC;SLO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT; GeneReviews:GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1505:C0338451:600274:282:230270009; NBK1161:NBK1236:C1843013:607822:1020
}}{{PMID Auto
|PMID=11094121
|Title=Dementia with prominent frontotemporal features associated with L113P presenilin 1 mutation.
}}