{{Rsnum
|rsid=12101255
|Gene=TSHR
|Chromosome=14
|position=80984708
|Orientation=plus
|GMAF=0.444
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=TSHR
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 41.4 | 49.5 | 9.0
| HCB | 13.1 | 46.0 | 40.9
| JPT | 15.0 | 55.8 | 29.2
| YRI | 36.1 | 46.3 | 17.7
| ASW | 36.8 | 50.9 | 12.3
| CHB | 13.1 | 46.0 | 40.9
| CHD | 4.6 | 55.0 | 40.4
| GIH | 52.5 | 37.6 | 9.9
| LWK | 17.3 | 59.1 | 23.6
| 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
|PMID=19244275
|Title=Association of the thyroid stimulating hormone receptor gene (TSHR) with Graves' disease
}}

{{PMID Auto
|PMID=21124799
|Title=Thyroid Stimulating Hormone Receptor (TSHR) Intron 1 Variants Are Major Risk Factors for Graves' Disease in Three European Caucasian Cohorts
|OA=1
}}

{{omim
|id=275000
|rsnum=12101255
}}

{{PMID Auto
|PMID=22673349
|Title=Association between thyroid stimulating hormone receptor gene intron polymorphisms and autoimmune thyroid disease in a Chinese Han population
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}