{{Rsnum
|rsid=690705
|Chromosome=13
|position=34080781
|Orientation=plus
|GMAF=0.3251
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 54.9 | 35.4 | 9.7
| HCB | 53.3 | 41.6 | 5.1
| JPT | 33.6 | 57.5 | 8.8
| YRI | 49.7 | 38.8 | 11.6
| ASW | 40.4 | 54.4 | 5.3
| CHB | 53.3 | 41.6 | 5.1
| CHD | 60.6 | 36.7 | 2.8
| GIH | 56.4 | 38.6 | 5.0
| LWK | 52.7 | 40.0 | 7.3
| MEX | 27.6 | 48.3 | 24.1
| MKK | 66.0 | 29.5 | 4.5
| TSI | 46.1 | 44.1 | 9.8
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=19749422
|Trait=Alzheimer's Disease
|Title=Genome-Wide Scan of Copy Number Variation in Late-Onset Alzheimer's Disease
|RiskAllele=
|Pval=6E-7
|OR=NR
|ORtxt=NR
}}

{{PMID Auto GWAS
|PMID=20061627
|Trait=Alzheimer's disease
|Title=Genome-wide scan of copy number variation in late-onset Alzheimer's disease.
|RiskAllele=
|Pval=6E-7
|OR=None
|ORtxt=None
|OA=1
}}

{{GET Evidence
|impact=pathogenic
|qualified_impact=Insufficiently evaluated pathogenic
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs690705
|overall_frequency_n=45
|overall_frequency_d=128
|overall_frequency=0.351562
|n_genomes=32
|n_genomes_annotated=0
|n_haplomes=44
|n_articles=0
|n_articles_annotated=0
|in_gwas=Y
|autoscore=1
|webscore=N
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}