{{Rsnum
|rsid=1881747
|Chromosome=10
|position=54333575
|Orientation=plus
|GMAF=0.4757
|Assembly=GRCh37
|GenomeBuild=37.1
|dbSNPBuild=131
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
}}
{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 5.3 | 33.6 | 61.1
| HCB | 79.6 | 17.5 | 2.9
| JPT | 82.3 | 16.8 | 0.9
| YRI | 23.8 | 49.0 | 27.2
| ASW | 17.5 | 49.1 | 33.3
| CHB | 79.6 | 17.5 | 2.9
| CHD | 83.5 | 15.6 | 0.9
| GIH | 19.8 | 54.5 | 25.7
| LWK | 33.0 | 48.6 | 18.3
| MEX | 36.8 | 40.4 | 22.8
| MKK | 14.7 | 47.4 | 37.8
| TSI | 1.0 | 35.3 | 63.7
| HapMapRevision=28
}}Nominally significant association found for this SNP with late-onset [[Alzheimer's disease]] (odds ratio 1.24, p=0.011) in a study of ~1000 Caucasian patients, but it would not have withstood statistical correction for multiple testing. {{PMID|18163421}}

{{PMID Auto
|PMID=21281506
|Title=A unified framework for multi-locus association analysis of both common and rare variants.
|OA=1
}}

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