{{Rsnum
|rsid=1456988
|Chromosome=14
|position=98021670
|Orientation=plus
|GMAF=0.4192
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
}}{{ population diversity
| geno1=(G;G)
| geno2=(G;T)
| geno3=(T;T)
| CEU | 8.8 | 33.6 | 57.5
| HCB | 28.2 | 49.6 | 22.1
| JPT | 17.0 | 44.6 | 38.4
| YRI | 41.5 | 38.8 | 19.7
| ASW | 38.6 | 50.9 | 10.5
| CHB | 28.2 | 49.6 | 22.1
| CHD | 37.0 | 43.5 | 19.4
| GIH | 30.0 | 50.0 | 20.0
| LWK | 27.5 | 46.8 | 25.7
| MEX | 15.8 | 35.1 | 49.1
| MKK | 29.5 | 47.4 | 23.1
| TSI | 4.0 | 42.0 | 54.0
| 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=5E-9
  |OR=1.12
  |ORtxt=[1.09-1.18]
  }}

{{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}}