{{Rsnum
|rsid=669607
|Chromosome=3
|position=28029953
|Orientation=minus
|GMAF=0.3889
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
}}{{ population diversity
| geno1=(G;G)
| geno2=(G;T)
| geno3=(T;T)
| CEU | 30.1 | 37.2 | 32.7
| HCB | 16.2 | 54.4 | 29.4
| JPT | 23.9 | 46.0 | 30.1
| YRI | 1.4 | 13.6 | 85.0
| ASW | 1.8 | 35.1 | 63.2
| CHB | 16.2 | 54.4 | 29.4
| CHD | 18.3 | 55.0 | 26.6
| GIH | 17.8 | 42.6 | 39.6
| LWK | 0.0 | 19.1 | 80.9
| MEX | 17.5 | 50.9 | 31.6
| MKK | 3.8 | 33.3 | 62.8
| TSI | 33.3 | 51.0 | 15.7
| HapMapRevision=28
}}[http://blog.23andme.com/2011/09/06/snpwatch-new-associations-found-for-multiple-sclerosis/ 23andMe blog] [[multiple sclerosis]] C 1.15x

{{PMID Auto GWAS
|PMID=21833088
|Trait=None
|Title=Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis.
|RiskAllele=C
|Pval=2E-15
|OR=1.1300
|ORtxt=[1.12-1.15]
|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}}