{{Rsnum
|rsid=7539409
|Chromosome=1
|position=83789052
|Orientation=plus
|GMAF=0.08173
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=RP11-475O6.1
|Gene_s=RP11-475O6.1
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 69.0 | 31.0 | 0.0
| HCB | 90.5 | 9.5 | 0.0
| JPT | 91.1 | 8.9 | 0.0
| YRI | 100.0 | 0.0 | 0.0
| ASW | 89.3 | 10.7 | 0.0
| CHB | 90.5 | 9.5 | 0.0
| CHD | 87.2 | 12.8 | 0.0
| GIH | 78.0 | 19.0 | 3.0
| LWK | 98.2 | 1.8 | 0.0
| MEX | 75.9 | 24.1 | 0.0
| MKK | 80.0 | 19.4 | 0.6
| TSI | 83.0 | 17.0 | 0.0
| 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=0.000001
|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=0.000001
|OR=None
|ORtxt=None
|OA=1
}}

{{GET Evidence
|impact=pathogenic
|qualified_impact=Insufficiently evaluated pathogenic
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs7539409
|overall_frequency_n=116
|overall_frequency_d=128
|overall_frequency=0.90625
|n_genomes=55
|n_genomes_annotated=0
|n_haplomes=102
|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}}