{{Rsnum
|rsid=2294025
|Gene=TG
|Chromosome=8
|position=133133268
|Orientation=plus
|GMAF=0.4151
|Gene_s=TG
|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 | 18.6 | 53.1 | 28.3
| HCB | 3.6 | 39.4 | 56.9
| JPT | 0.0 | 15.9 | 84.1
| YRI | 30.6 | 54.4 | 15.0
| ASW | 21.1 | 54.4 | 24.6
| CHB | 3.6 | 39.4 | 56.9
| CHD | 4.6 | 23.9 | 71.6
| GIH | 6.9 | 41.6 | 51.5
| LWK | 32.7 | 45.5 | 21.8
| MEX | 19.0 | 48.3 | 32.8
| MKK | 30.1 | 49.4 | 20.5
| TSI | 23.5 | 49.0 | 27.5
| HapMapRevision=28
}}{{PMID Auto GWAS
  |PMID=23612905
  |Trait=Graves' disease
  |Title=Robust evidence for five new Graves' disease risk loci from a staged genome-wide association analysis.
  |RiskAllele=T
  |Pval=8E-9
  |OR=1.16
  |ORtxt=[1.10-1.22]
  }}

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