{{Rsnum
|rsid=6887649
|Chromosome=5
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|position=121842820
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 89.4 | 9.7 | 0.9
| HCB | 72.8 | 26.5 | 0.7
| JPT | 75.2 | 23.0 | 1.8
| YRI | 51.4 | 39.0 | 9.6
| ASW | 49.1 | 43.9 | 7.0
| CHB | 72.8 | 26.5 | 0.7
| CHD | 85.3 | 13.8 | 0.9
| GIH | 87.1 | 12.9 | 0.0
| LWK | 55.5 | 36.4 | 8.2
| MEX | 77.2 | 21.1 | 1.8
| MKK | 54.8 | 39.4 | 5.8
| TSI | 89.2 | 9.8 | 1.0
| HapMapRevision=28
}}{{PMID Auto
|PMID=25140149
|Title=Genetic variation modifies risk for neurodegeneration based on biomarker status
}}

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