{{Rsnum
|rsid=3135338
|Chromosome=6
|position=32433440
|Orientation=minus
|GMAF=0.3705
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 39.8 | 46.0 | 14.2
| HCB | 56.2 | 37.2 | 6.6
| JPT | 43.4 | 37.2 | 19.5
| YRI | 21.1 | 47.6 | 31.3
| ASW | 29.8 | 40.4 | 29.8
| CHB | 56.2 | 37.2 | 6.6
| CHD | 54.1 | 42.2 | 3.7
| GIH | 43.6 | 40.6 | 15.8
| LWK | 25.5 | 40.9 | 33.6
| MEX | 44.8 | 50.0 | 5.2
| MKK | 31.4 | 48.7 | 19.9
| TSI | 44.1 | 46.1 | 9.8
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=20159113
|Trait=Multiple sclerosis
|Title=Genome-wide Association Study in a High-Risk Isolate for Multiple Sclerosis Reveals Associated Variants in STAT3 Gene
|RiskAllele=A
|Pval=2E-25
|OR=3.43
|ORtxt=[NR]
|OA=1
}}

{{PMID Auto
|PMID=19143815
|Title=MHC fine mapping of human type 1 diabetes using the T1DGC data.
|OA=1
}}

{{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}}