{{Rsnum
|rsid=4947296
|Chromosome=6
|position=31090401
|Orientation=plus
|GMAF=0.09504
|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 | 0.0 | 12.4 | 87.6
| HCB | 3.7 | 31.3 | 64.9
| JPT | 4.4 | 26.7 | 68.9
| YRI | 0.0 | 0.7 | 99.3
| ASW | 0.0 | 3.5 | 96.5
| CHB | 3.7 | 31.3 | 64.9
| CHD | 4.7 | 27.4 | 67.9
| GIH | 1.0 | 26.7 | 72.3
| LWK | 0.0 | 0.0 | 0.0
| MEX | 1.8 | 8.8 | 89.5
| MKK | 0.7 | 13.9 | 85.4
| TSI | 1.0 | 17.6 | 81.4
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=21841780
|Trait=None
|Title=A genome-wide association study identifies two new risk loci for Graves' disease.
|RiskAllele=C
|Pval=4E-51
|OR=1.7700
|ORtxt=[1.65-1.91]
}}

{{PMID Auto GWAS
  |PMID=23001997
  |Trait=Behcet's disease
  |Title=Identification of a susceptibility locus in STAT4 for Behçet's disease in Han Chinese in a genome-wide association study.
  |RiskAllele=
  |Pval=1E-11
  |OR=2.57
  |ORtxt=[1.96-3.37]
  }}

{{PMID Auto
|PMID=23667180
|Title=An X chromosome-wide association analysis identifies variants in GPR174 as a risk factor for Graves' disease.
|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}}