{{Rsnum
|rsid=2069550
|Gene=TG
|Chromosome=8
|position=132888141
|Orientation=plus
|ReferenceAllele=T
|GMAF=0.3623
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=TG
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 20.4 | 49.6 | 30.1
| HCB | 61.8 | 30.1 | 8.1
| JPT | 53.6 | 42.9 | 3.6
| YRI | 59.9 | 34.0 | 6.1
| ASW | 59.6 | 31.6 | 8.8
| CHB | 61.8 | 30.1 | 8.1
| CHD | 57.8 | 34.9 | 7.3
| GIH | 54.5 | 37.6 | 7.9
| LWK | 50.9 | 40.0 | 9.1
| MEX | 25.9 | 60.3 | 13.8
| MKK | 57.7 | 34.0 | 8.3
| TSI | 31.4 | 51.0 | 17.6
| HapMapRevision=28
}}
{{PMID Auto
|PMID=19438904
|Title=Clinical associations of the genetic variants of CTLA-4, Tg, TSHR, PTPN22, PTPN12 and FCRL3 in patients with Graves' disease
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}