{{Rsnum
|rsid=9275563
|Chromosome=6
|position=32710135
|Orientation=plus
|GMAF=0.4403
|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 | 24.3 | 50.5 | 25.2
| HCB | 32.8 | 38.9 | 28.2
| JPT | 21.8 | 53.6 | 24.5
| YRI | 39.4 | 49.3 | 11.3
| ASW | 26.8 | 55.4 | 17.9
| CHB | 32.8 | 38.9 | 28.2
| CHD | 0.0 | 0.0 | 0.0
| GIH | 16.3 | 48.0 | 35.7
| LWK | 48.1 | 41.5 | 10.4
| MEX | 0.0 | 0.0 | 0.0
| MKK | 28.7 | 54.0 | 17.3
| TSI | 31.3 | 35.4 | 33.3
| HapMapRevision=28
}}{{PMID Auto GWAS
  |PMID=23472185
  |Trait=Multiple sclerosis (OCB status)
  |Title=Oligoclonal band status in Scandinavian multiple sclerosis patients is associated with specific genetic risk alleles.
  |RiskAllele=
  |Pval=6E-11
  |OR=1.75
  |ORtxt=[1.47-2.04]
  |OA=1
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}