{{Rsnum
|rsid=3893464
|Gene=HCG2P6
|Chromosome=6
|position=29967473
|Orientation=minus
|GMAF=0.4761
|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 | 25.9 | 54.5 | 19.6
| HCB | 21.1 | 43.6 | 35.3
| JPT | 13.8 | 41.3 | 45.0
| YRI | 23.8 | 54.0 | 22.2
| ASW | 43.9 | 47.4 | 8.8
| CHB | 21.1 | 43.6 | 35.3
| CHD | 10.3 | 55.1 | 34.6
| GIH | 13.0 | 40.0 | 47.0
| LWK | 47.7 | 39.3 | 13.1
| MEX | 31.0 | 55.2 | 13.8
| MKK | 35.1 | 46.8 | 18.2
| TSI | 27.0 | 54.0 | 19.0
| 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=G
|Pval=2E-20
|OR=1.5300
|ORtxt=[1.39-1.67]
}}

{{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}}