{{Rsnum
|rsid=2142991
|Chromosome=10
|position=43341105
|Orientation=minus
|GMAF=0.1414
|Assembly=GRCh37
|GenomeBuild=37.1
|dbSNPBuild=132
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
}}
{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 69.9 | 27.4 | 2.7
| HCB | 76.6 | 21.9 | 1.5
| JPT | 71.7 | 26.5 | 1.8
| YRI | 89.8 | 10.2 | 0.0
| ASW | 75.4 | 22.8 | 1.8
| CHB | 76.6 | 21.9 | 1.5
| CHD | 72.5 | 25.7 | 1.8
| GIH | 69.0 | 29.0 | 2.0
| LWK | 92.7 | 7.3 | 0.0
| MEX | 79.3 | 19.0 | 1.7
| MKK | 82.1 | 16.7 | 1.3
| TSI | 65.7 | 32.4 | 2.0
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=21685912
|Trait=None
|Title=Identification of common variants influencing risk of the tauopathy progressive supranuclear palsy.
|RiskAllele=
|Pval=3E-7
|OR=1.3000
|ORtxt=[1.18-1.44]
|OA=1
}}

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