{{Rsnum
|rsid=9390537
|Chromosome=6
|position=148102235
|Orientation=plus
|GMAF=0.3774
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 2.7 | 36.3 | 61.1
| HCB | 38.7 | 49.6 | 11.7
| JPT | 39.8 | 41.6 | 18.6
| YRI | 6.1 | 42.2 | 51.7
| ASW | 8.8 | 42.1 | 49.1
| CHB | 38.7 | 49.6 | 11.7
| CHD | 48.1 | 42.6 | 9.3
| GIH | 24.8 | 42.6 | 32.7
| LWK | 6.4 | 36.4 | 57.3
| MEX | 31.0 | 48.3 | 20.7
| MKK | 6.4 | 34.6 | 59.0
| TSI | 4.9 | 32.4 | 62.7
| 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=0.000008
|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=0.000008
|OR=None
|ORtxt=None
|OA=1
}}

{{GET Evidence
|impact=pathogenic
|qualified_impact=Insufficiently evaluated pathogenic
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs9390537
|overall_frequency_n=85
|overall_frequency_d=116
|overall_frequency=0.732759
|n_genomes=43
|n_genomes_annotated=0
|n_haplomes=73
|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 | Affy GenomeWide 6}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}