{{Rsnum
|rsid=11129640
|Chromosome=3
|position=35101019
|Orientation=plus
|GMAF=0.2383
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene=LOC101928135
|Gene_s=LOC101928135
}}{{ population diversity
| geno1=(G;G)
| geno2=(G;T)
| geno3=(T;T)
| CEU | 50.4 | 43.4 | 6.2
| HCB | 46.7 | 44.5 | 8.8
| JPT | 53.1 | 38.9 | 8.0
| YRI | 63.9 | 30.6 | 5.4
| ASW | 56.1 | 38.6 | 5.3
| CHB | 46.7 | 44.5 | 8.8
| CHD | 56.9 | 36.7 | 6.4
| GIH | 24.8 | 57.4 | 17.8
| LWK | 55.5 | 39.1 | 5.5
| MEX | 56.9 | 39.7 | 3.4
| MKK | 54.5 | 37.2 | 8.3
| TSI | 55.4 | 41.6 | 3.0
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=21116278
|Trait=None
|Title=Genome-wide association with MRI atrophy measures as a quantitative trait locus for Alzheimer's disease
|RiskAllele=
|Pval=6E-8
|OR=0.1232
|ORtxt=[NR] unit decrease (main effect)
}}

{{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 | FTDNA}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}