{{Rsnum
|rsid=650258
|Chromosome=11
|position=61064810
|Orientation=plus
|GMAF=0.2773
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 33.9 | 59.8 | 6.2
| HCB | 81.0 | 18.2 | 0.7
| JPT | 88.5 | 11.5 | 0.0
| YRI | 44.9 | 42.9 | 12.2
| ASW | 40.4 | 50.9 | 8.8
| CHB | 81.0 | 18.2 | 0.7
| CHD | 75.2 | 20.2 | 4.6
| GIH | 45.5 | 44.6 | 9.9
| LWK | 42.7 | 46.4 | 10.9
| MEX | 58.9 | 35.7 | 5.4
| MKK | 34.6 | 52.6 | 12.8
| TSI | 40.2 | 44.1 | 15.7
| HapMapRevision=28
}}{{PMID Auto GWAS
  |PMID=21833088
  |Trait=Multiple sclerosis
  |Title=Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis.
  |RiskAllele=G
  |Pval=2E-11
  |OR=1.12
  |ORtxt=[1.1-1.13]
  |OA=1
}}

{{PMID Auto
|PMID=23638056
|Title=Fine Mapping and Functional Analysis of the Multiple Sclerosis Risk Gene CD6
|OA=1
}}

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