{{Rsnum
|rsid=4248154
|Gene=MUC22
|Chromosome=6
|position=31034839
|Orientation=plus
|GMAF=0.2043
|Gene_s=MUC22
|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 | 67.3 | 27.4 | 5.3
| HCB | 56.6 | 36.8 | 6.6
| JPT | 27.4 | 51.3 | 21.2
| YRI | 78.8 | 17.8 | 3.4
| ASW | 71.9 | 26.3 | 1.8
| CHB | 56.6 | 36.8 | 6.6
| CHD | 46.8 | 45.9 | 7.3
| GIH | 64.4 | 31.7 | 4.0
| LWK | 81.8 | 15.5 | 2.7
| MEX | 74.1 | 22.4 | 3.4
| MKK | 89.1 | 10.9 | 0.0
| TSI | 73.5 | 26.5 | 0.0
| 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=C
|Pval=1E-13
|OR=1.3800
|ORtxt=[1.27-1.50]
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | FTDNA2}}
{{on chip | FTDNA}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}