{{Rsnum
|rsid=386965
|Chromosome=16
|position=79618644
|Orientation=minus
|GMAF=0.3737
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 62.8 | 31.9 | 5.3
| HCB | 25.5 | 46.7 | 27.7
| JPT | 23.9 | 47.8 | 28.3
| YRI | 37.4 | 45.6 | 17.0
| ASW | 36.8 | 47.4 | 15.8
| CHB | 25.5 | 46.7 | 27.7
| CHD | 29.4 | 45.0 | 25.7
| GIH | 38.6 | 49.5 | 11.9
| LWK | 41.8 | 45.5 | 12.7
| MEX | 37.9 | 50.0 | 12.1
| MKK | 45.5 | 44.9 | 9.6
| TSI | 62.7 | 35.3 | 2.0
| 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=4E-6
  |OR=1.09
  |ORtxt=[1.07-1.11]
  |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 | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}