{{Rsnum
|rsid=13333054
|Chromosome=16
|position=85977427
|Orientation=plus
|GMAF=0.3017
|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 | 61.1 | 36.3 | 2.7
| HCB | 27.7 | 52.6 | 19.7
| JPT | 38.4 | 42.9 | 18.8
| YRI | 60.3 | 34.9 | 4.8
| ASW | 66.7 | 28.1 | 5.3
| CHB | 27.7 | 52.6 | 19.7
| CHD | 28.0 | 46.7 | 25.2
| GIH | 70.0 | 27.0 | 3.0
| LWK | 60.9 | 35.5 | 3.6
| MEX | 43.1 | 43.1 | 13.8
| MKK | 50.6 | 39.7 | 9.6
| TSI | 55.4 | 38.6 | 5.9
| 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=A
  |Pval=1E-8
  |OR=1.11
  |ORtxt=[1.1-1.13]
  |OA=1
}}

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