{{Rsnum
|rsid=12101261
|Gene=TSHR
|Chromosome=14
|position=80984885
|Orientation=plus
|GMAF=0.4449
|Gene_s=TSHR
|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 | 40.7 | 49.6 | 9.7
| HCB | 13.1 | 46.0 | 40.9
| JPT | 15.0 | 55.8 | 29.2
| YRI | 36.7 | 45.6 | 17.7
| ASW | 36.8 | 49.1 | 14.0
| CHB | 13.1 | 46.0 | 40.9
| CHD | 4.6 | 55.0 | 40.4
| GIH | 52.5 | 37.6 | 9.9
| LWK | 17.4 | 59.6 | 22.9
| MEX | 24.1 | 53.4 | 22.4
| MKK | 41.0 | 47.4 | 11.5
| TSI | 44.1 | 46.1 | 9.8
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=21841780
|Trait=None
|Title=A genome-wide association study identifies two new risk loci for Graves' disease.
|RiskAllele=T
|Pval=7E-24
|OR=1.3500
|ORtxt=[1.28-1.43]
}}

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