{{Rsnum
|rsid=1082714
|Chromosome=12
|position=67235051
|Orientation=plus
|GMAF=0.4702
|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 | 44.1 | 49.5 | 6.3
| HCB | 17.5 | 51.1 | 31.4
| JPT | 22.3 | 54.5 | 23.2
| YRI | 4.8 | 36.3 | 58.9
| ASW | 10.5 | 36.8 | 52.6
| CHB | 17.5 | 51.1 | 31.4
| CHD | 20.4 | 41.7 | 38.0
| GIH | 51.5 | 43.6 | 5.0
| LWK | 7.3 | 31.8 | 60.9
| MEX | 60.7 | 30.4 | 8.9
| MKK | 18.7 | 52.9 | 28.4
| TSI | 64.7 | 27.5 | 7.8
| 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=0.000005
|OR=NR
|ORtxt=NR
|OA=1
}}

{{GET Evidence
|impact=pathogenic
|qualified_impact=Insufficiently evaluated pathogenic
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs1082714
|overall_frequency_n=57
|overall_frequency_d=124
|overall_frequency=0.459677
|n_genomes=36
|n_genomes_annotated=0
|n_haplomes=52
|n_articles=0
|n_articles_annotated=0
|in_gwas=Y
|autoscore=1
|webscore=N
}}

{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | Illumina Human 1M}}