{{Rsnum
|rsid=63749884
|Chromosome=1
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=PSEN2
|position=226888979
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=PSEN2
}}{{omim
|id=600759
|rsnum=63749884
|variant=0006
}}

{{ClinVar
|rsid=63749884
|Reversed=0
|FwdREF=G
|FwdALT=A
|REF=G
|ALT=A
|RSPOS=226888979
|CHROM=1
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050168000a05000002110100
|GENEINFO=PSEN2:5664
|GENE_NAME=PSEN2
|GENE_ID=5664
|WGT=1
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000001.11:g.226888979G>A
|CLNSRC=ClinVar; GeneReviews; Neurodegenerative Brain Diseases Group; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NM_000447.2:c.717G>A; NBK1236; ADM_77; 600759.0006
|CLNSIG=5
|CLNCUI=C1847200
|CLNDBN=Alzheimer disease, type 4; not provided
|Disease=Alzheimer disease; not provided
|CLNACC=RCV000009398.2; RCV000084266.1
|Tags=PM;PMC;SLO;NSM;REF;ASP;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1236:C1847200:606889:ORPHA1020
}}

{{PMID Auto
|PMID=7651536
|Title=Familial Alzheimer's disease in kindreds with missense mutations in a gene on chromosome 1 related to the Alzheimer's disease type 3 gene.
}}

{{PMID Auto
|PMID=15055444
|Title=Neuropathological and clinical phenotype of an Italian Alzheimer family with M239V mutation of presenilin 2 gene.
}}

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