{{Rsnum
|rsid=4713693
|Chromosome=6
|position=33850152
|Orientation=plus
|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 | 10.6 | 50.4 | 38.9
| HCB | 6.6 | 39.4 | 54.0
| JPT | 14.2 | 46.0 | 39.8
| YRI | 23.8 | 51.0 | 25.2
| ASW | 24.6 | 50.9 | 24.6
| CHB | 6.6 | 39.4 | 54.0
| CHD | 6.4 | 43.1 | 50.5
| GIH | 11.9 | 34.7 | 53.5
| LWK | 32.7 | 52.7 | 14.5
| MEX | 8.8 | 47.4 | 43.9
| MKK | 45.5 | 48.7 | 5.8
| TSI | 28.4 | 47.1 | 24.5
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=21900946
|Trait=None
|Title=Identification of independent risk loci for Graves' disease within the MHC in the Japanese population.
|RiskAllele=T
|Pval=7E-13
|OR=1.4000
|ORtxt=[1.28-1.53]
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}