{{Rsnum
|rsid=3129720
|Chromosome=6
|position=32695854
|Orientation=plus
|GMAF=0.2039
|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 | 52.4 | 36.5 | 11.1
| HCB | 84.1 | 13.6 | 2.3
| JPT | 66.7 | 26.7 | 6.7
| YRI | 61.3 | 33.9 | 4.8
| ASW | 0.0 | 0.0 | 0.0
| CHB | 84.1 | 13.6 | 2.3
| CHD | 0.0 | 0.0 | 0.0
| GIH | 0.0 | 0.0 | 0.0
| LWK | 0.0 | 0.0 | 0.0
| MEX | 0.0 | 0.0 | 0.0
| MKK | 0.0 | 0.0 | 0.0
| TSI | 0.0 | 0.0 | 0.0
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=22493691
|Trait=None
|Title=Novel associations for hypothyroidism include known autoimmune risk loci.
|RiskAllele=C
|Pval=5E-7
|OR=1.1600
|ORtxt=None
|OA=1
}}

{{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=5E-15
  |OR=1.91
  |ORtxt=[1.62-2.24]
  |OA=1
}}

{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | HumanOmni1Quad}}