{{Rsnum
|rsid=9891119
|Gene=STAT3
|Chromosome=17
|position=42355962
|Orientation=plus
|GMAF=0.3714
|Gene_s=STAT3
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;C)
| geno3=(C;C)
| CEU | 40.7 | 40.7 | 18.6
| HCB | 41.9 | 44.9 | 13.2
| JPT | 34.5 | 49.6 | 15.9
| YRI | 32.0 | 46.9 | 21.1
| ASW | 31.6 | 52.6 | 15.8
| CHB | 41.9 | 44.9 | 13.2
| CHD | 33.0 | 52.3 | 14.7
| GIH | 29.7 | 44.6 | 25.7
| LWK | 33.6 | 44.5 | 21.8
| MEX | 56.9 | 37.9 | 5.2
| MKK | 19.2 | 40.4 | 40.4
| TSI | 40.2 | 47.1 | 12.7
| HapMapRevision=28
}}{{PMID Auto GWAS
  |PMID=23266558
  |Trait=Crohn's disease
  |Title=A Genome-Wide Association Study Identifies 2 Susceptibility Loci for Crohn's Disease in a Japanese Population.
  |RiskAllele=A
  |Pval=2E-15
  |OR=1.37
  |ORtxt=[1.27-1.48]
  }}

{{PMID Auto GWAS
  |PMID=21833088
  |Trait=Multiple sclerosis
  |Title=Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis.
  |RiskAllele=C
  |Pval=2E-10
  |OR=1.11
  |ORtxt=[1.09-1.12]
  |OA=1
}}

{{PMID Auto
|PMID=18451776
|Title=Study of genetic variation in the STAT3 on obesity and insulin resistance in male adults.
}}

{{PMID Auto
|PMID=18789715
|Title=Genetic variants in STAT3 are associated with nonalcoholic fatty liver disease.
}}

{{PMID Auto
|PMID=21310444
|Title=Mitochondrial DNA copy number is modulated by genetic variation in the signal transducer and activator of transcription 3 (STAT3).
}}

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