{{Rsnum
|rsid=6590322
|Chromosome=11
|position=128336515
|Orientation=plus
|GMAF=0.4931
|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 | 17.9 | 47.3 | 34.8
| HCB | 27.0 | 43.8 | 29.2
| JPT | 36.3 | 45.1 | 18.6
| YRI | 28.6 | 55.1 | 16.3
| ASW | 26.3 | 52.6 | 21.1
| CHB | 27.0 | 43.8 | 29.2
| CHD | 22.0 | 48.6 | 29.4
| GIH | 21.8 | 39.6 | 38.6
| LWK | 35.5 | 53.6 | 10.9
| MEX | 46.6 | 32.8 | 20.7
| MKK | 40.4 | 43.6 | 16.0
| TSI | 15.7 | 52.0 | 32.4
| 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=0.000009
|OR=NR
|ORtxt=NR
|OA=1
}}

{{GET Evidence
|impact=pathogenic
|qualified_impact=Insufficiently evaluated pathogenic
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs6590322
|overall_frequency_n=63
|overall_frequency_d=126
|overall_frequency=0.5
|n_genomes=41
|n_genomes_annotated=0
|n_haplomes=57
|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 | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}