{{Rsnum
|rsid=4509693
|Chromosome=10
|position=102501571
|Orientation=plus
|GMAF=0.1708
|Assembly=GRCh37
|GenomeBuild=37.1
|dbSNPBuild=131
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
}}
{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 3.5 | 36.3 | 60.2
| HCB | 0.0 | 1.5 | 98.5
| JPT | 0.0 | 0.0 | 100.0
| YRI | 9.6 | 38.4 | 52.1
| ASW | 10.5 | 28.1 | 61.4
| CHB | 0.0 | 1.5 | 98.5
| CHD | 0.0 | 0.0 | 0.0
| GIH | 0.0 | 6.9 | 93.1
| LWK | 11.0 | 49.5 | 39.4
| MEX | 3.4 | 27.6 | 69.0
| MKK | 9.0 | 51.3 | 39.7
| TSI | 6.9 | 33.3 | 59.8
| 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=0.000006
|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=0.000006
|OR=None
|ORtxt=None
|OA=1
}}

{{GET Evidence
|impact=pathogenic
|qualified_impact=Insufficiently evaluated pathogenic
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs4509693
|overall_frequency_n=104
|overall_frequency_d=128
|overall_frequency=0.8125
|n_genomes=52
|n_genomes_annotated=0
|n_haplomes=90
|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 | Illumina Human 1M}}