{{Rsnum
|rsid=5912838
|Chromosome=X
|position=79241621
|Orientation=plus
|GMAF=0.4849
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;C)
| geno3=(C;C)
| CEU | 34.9 | 23.8 | 41.3
| HCB | 46.5 | 25.6 | 27.9
| JPT | 44.2 | 23.3 | 32.6
| YRI | 32.3 | 33.9 | 33.9
| ASW | 0.0 | 0.0 | 0.0
| CHB | 46.5 | 25.6 | 27.9
| 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 Auto GWAS
  |PMID=23612905
  |Trait=Graves' disease
  |Title=Robust evidence for five new Graves' disease risk loci from a staged genome-wide association analysis.
  |RiskAllele=
  |Pval=2E-33
  |OR=1.32
  |ORtxt=[1.25-1.37]
  }}

{{PMID Auto
|PMID=23667180
|Title=An X chromosome-wide association analysis identifies variants in GPR174 as a risk factor for Graves' disease.
|OA=1
}}

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