{{Rsnum
|rsid=11129295
|Chromosome=3
|position=27747289
|Orientation=plus
|GMAF=0.494
|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 | 38.9 | 49.6 | 11.5
| HCB | 7.3 | 38.0 | 54.7
| JPT | 6.2 | 30.1 | 63.7
| YRI | 51.0 | 40.1 | 8.8
| ASW | 38.6 | 56.1 | 5.3
| CHB | 7.3 | 38.0 | 54.7
| CHD | 0.0 | 45.0 | 55.0
| GIH | 7.9 | 33.7 | 58.4
| LWK | 43.6 | 38.2 | 18.2
| MEX | 13.8 | 48.3 | 37.9
| MKK | 35.3 | 42.9 | 21.8
| TSI | 34.3 | 52.9 | 12.7
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=21833088
|Trait=None
|Title=Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis.
|RiskAllele=A
|Pval=1E-9
|OR=1.1100
|ORtxt=[1.09-1.12]
|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 | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}
{{on chip | NatGeo2}}