{{Rsnum
|rsid=10867752
|Chromosome=9
|position=81400122
|Orientation=plus
|GMAF=0.08815
|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 | 71.7 | 24.8 | 3.5
| HCB | 93.4 | 6.6 | 0.0
| JPT | 90.3 | 9.7 | 0.0
| YRI | 100.0 | 0.0 | 0.0
| ASW | 94.6 | 5.4 | 0.0
| CHB | 93.4 | 6.6 | 0.0
| CHD | 91.7 | 8.3 | 0.0
| GIH | 87.1 | 12.9 | 0.0
| LWK | 98.2 | 1.8 | 0.0
| MEX | 86.0 | 12.3 | 1.8
| MKK | 95.5 | 4.5 | 0.0
| TSI | 72.5 | 21.6 | 5.9
| HapMapRevision=28
}}
{{PMID Auto GWAS
|PMID=19668339
|Trait=Hippocampal atrophy
|Title=Hippocampal atrophy as a quantitative trait in a genome-wide association study identifying novel susceptibility genes for Alzheimer's disease
|RiskAllele=
|Pval=0.000003
|OR=NR
|ORtxt=NR
|OA=1
}}

{{GET Evidence
|impact=pathogenic
|qualified_impact=Insufficiently evaluated pathogenic
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs10867752
|overall_frequency_n=11
|overall_frequency_d=128
|overall_frequency=0.0859375
|n_genomes=8
|n_genomes_annotated=0
|n_haplomes=8
|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 | Illumina Human 1M}}