{{Rsnum
|rsid=6547705
|Gene=CD8B
|Chromosome=2
|position=86817193
|Orientation=plus
|GMAF=0.1253
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=CD8B
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 63.7 | 34.5 | 1.8
| HCB | 97.1 | 2.9 | 0.0
| JPT | 92.0 | 8.0 | 0.0
| YRI | 96.6 | 3.4 | 0.0
| ASW | 94.7 | 5.3 | 0.0
| CHB | 97.1 | 2.9 | 0.0
| CHD | 96.3 | 3.7 | 0.0
| GIH | 36.6 | 47.5 | 15.8
| LWK | 94.5 | 5.5 | 0.0
| MEX | 56.9 | 37.9 | 5.2
| MKK | 87.2 | 12.8 | 0.0
| TSI | 52.0 | 42.2 | 5.9
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=21685912
|Trait=None
|Title=Identification of common variants influencing risk of the tauopathy progressive supranuclear palsy.
|RiskAllele=
|Pval=1E-8
|OR=1.2800
|ORtxt=[1.18-1.40]
|OA=1
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | FTDNA}}
{{on chip | Illumina Human 1M}}
{{on chip | NatGeo2}}