{{Rsnum
|rsid=4667682
|Chromosome=2
|position=171271410
|Orientation=plus
|GMAF=0.225
|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 | 75.9 | 21.4 | 2.7
| HCB | 28.7 | 53.7 | 17.6
| JPT | 35.4 | 45.1 | 19.5
| YRI | 92.4 | 6.2 | 1.4
| ASW | 84.2 | 15.8 | 0.0
| CHB | 28.7 | 53.7 | 17.6
| CHD | 35.8 | 46.8 | 17.4
| GIH | 64.4 | 33.7 | 2.0
| LWK | 89.8 | 10.2 | 0.0
| MEX | 51.7 | 41.4 | 6.9
| MKK | 73.7 | 25.6 | 0.6
| TSI | 72.3 | 20.8 | 6.9
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=22745009
|Trait=None
|Title=Multiple loci influencing hippocampal degeneration identified by genome scan.
|RiskAllele=C
|Pval=0.000005
|OR=None
|ORtxt=None
|OA=1
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}