{{Rsnum
|rsid=179247
|Gene=TSHR
|Chromosome=14
|position=80966202
|Orientation=plus
|GMAF=0.3806
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=TSHR
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 23.0 | 57.5 | 19.5
| HCB | 43.1 | 46.0 | 10.9
| JPT | 30.1 | 55.8 | 14.2
| YRI | 81.5 | 15.8 | 2.7
| ASW | 71.9 | 22.8 | 5.3
| CHB | 43.1 | 46.0 | 10.9
| CHD | 43.1 | 52.3 | 4.6
| GIH | 15.8 | 48.5 | 35.6
| LWK | 74.5 | 25.5 | 0.0
| MEX | 36.2 | 44.8 | 19.0
| MKK | 63.0 | 32.5 | 4.5
| TSI | 32.4 | 50.0 | 17.6
| 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=179247
}}

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

{{PMID Auto
|PMID=21642385
|Title=Association of an SNP with intrathymic transcription of TSHR and Graves' disease: a role for defective thymic tolerance.
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}