{{Rsnum
|rsid=2268458
|Gene=TSHR
|Chromosome=14
|position=80996551
|Orientation=plus
|GMAF=0.1988
|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 | 4.6 | 41.5 | 53.8
| HCB | 11.1 | 28.9 | 60.0
| JPT | 4.5 | 36.4 | 59.1
| YRI | 0.0 | 0.0 | 100.0
| ASW | 0.0 | 0.0 | 0.0
| CHB | 11.1 | 28.9 | 60.0
| CHD | 0.0 | 0.0 | 0.0
| GIH | 0.0 | 0.0 | 0.0
| LWK | 0.0 | 0.0 | 0.0
| MEX | 0.0 | 0.0 | 0.0
| MKK | 0.0 | 0.0 | 0.0
| TSI | 0.0 | 0.0 | 0.0
| HapMapRevision=28
}}

{{PMID|18925838|OA=1
}} [[rs2268458]] was associated with [[Graves' disease]]

{{omim
|desc=GRAVES DISEASE
|id=275000
|rsnum=2268458
}}

{{PMID Auto
|PMID=16106256
|Title=Association of the TSHR gene with Graves' disease: the first disease specific locus.
}}

{{PMID Auto
|PMID=17608818
|Title=Preliminary evidence for interaction of PTPN12 polymorphism with TSHR genotype and association with Graves' ophthalmopathy.
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}