{{Rsnum
|rsid=2273017
|Gene=C6orf10
|Chromosome=6
|position=32369853
|Orientation=minus
|GMAF=0.4826
|Gene_s=C6orf10
|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 | 17.9 | 48.2 | 33.9
| HCB | 12.6 | 43.0 | 44.4
| JPT | 23.0 | 46.9 | 30.1
| YRI | 61.0 | 31.5 | 7.5
| ASW | 52.6 | 42.1 | 5.3
| CHB | 12.6 | 43.0 | 44.4
| CHD | 12.8 | 49.5 | 37.6
| GIH | 12.9 | 43.6 | 43.6
| LWK | 50.5 | 42.2 | 7.3
| MEX | 8.6 | 53.4 | 37.9
| MKK | 35.9 | 50.0 | 14.1
| TSI | 14.9 | 48.5 | 36.6
| 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=A
|Pval=2E-22
|OR=1.5300
|ORtxt=[1.40-1.66]
}}

{{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}}