{{Rsnum
|rsid=233100
|Chromosome=1
|position=85306326
|Orientation=plus
|GMAF=0.4279
|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 | 32.7 | 52.2 | 15.0
| HCB | 19.7 | 48.2 | 32.1
| JPT | 31.0 | 51.3 | 17.7
| YRI | 55.8 | 36.1 | 8.2
| ASW | 50.9 | 42.1 | 7.0
| CHB | 19.7 | 48.2 | 32.1
| CHD | 19.3 | 59.6 | 21.1
| GIH | 51.5 | 42.6 | 5.9
| LWK | 43.6 | 42.7 | 13.6
| MEX | 31.0 | 58.6 | 10.3
| MKK | 42.9 | 48.1 | 9.0
| TSI | 31.4 | 46.1 | 22.5
| 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=G
|Pval=0.000001
|OR=1.0800
|ORtxt=[1.07-1.10]
|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}}