{{Rsnum
|rsid=1520333
|Chromosome=8
|position=78488803
|Orientation=minus
|GMAF=0.4151
|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 | 6.2 | 35.4 | 58.4
| HCB | 25.5 | 48.2 | 26.3
| JPT | 13.3 | 49.6 | 37.2
| YRI | 55.1 | 35.4 | 9.5
| ASW | 33.3 | 57.9 | 8.8
| CHB | 25.5 | 48.2 | 26.3
| CHD | 26.9 | 53.7 | 19.4
| GIH | 9.9 | 50.5 | 39.6
| LWK | 55.5 | 40.9 | 3.6
| MEX | 6.9 | 36.2 | 56.9
| MKK | 30.8 | 48.1 | 21.2
| TSI | 6.9 | 49.0 | 44.1
| 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=G
  |Pval=2E-7
  |OR=1.10
  |ORtxt=[1.08-1.11]
  |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 | Illumina Human 1M}}