{{Rsnum
|rsid=1597944
|Chromosome=2
|position=233595452
|Orientation=plus
|GMAF=0.4394
|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 | 23.0 | 53.1 | 23.9
| HCB | 18.4 | 47.1 | 34.6
| JPT | 15.9 | 50.4 | 33.6
| YRI | 67.8 | 30.8 | 1.4
| ASW | 66.7 | 31.6 | 1.8
| CHB | 18.4 | 47.1 | 34.6
| CHD | 19.3 | 45.0 | 35.8
| GIH | 9.9 | 39.6 | 50.5
| LWK | 60.9 | 37.3 | 1.8
| MEX | 20.7 | 55.2 | 24.1
| MKK | 0.0 | 0.0 | 0.0
| TSI | 22.5 | 55.9 | 21.6
| HapMapRevision=28
}}

{{ population diversity
| geno1 = (C;C)
| geno2 = (C;T)
| geno3 = (T;T)
| CEU | 16.7 | 65.0 | 18.3
| CHB | 15.6 | 57.8 | 26.7
| JPT | 15.9 | 54.5 | 29.5
| YRI | 63.3 | 33.3 | 3.3
}}

{{PMID Auto
|PMID=19010793
|Title=Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis.
}}

{{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}}