{{Rsnum
|rsid=3129763
|Chromosome=6
|position=32623148
|Orientation=plus
|GMAF=0.2094
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 2.7 | 19.5 | 77.9
| HCB | 5.1 | 24.3 | 70.6
| JPT | 0.0 | 14.2 | 85.8
| YRI | 8.8 | 33.3 | 57.8
| ASW | 7.0 | 24.6 | 68.4
| CHB | 5.1 | 24.3 | 70.6
| CHD | 0.9 | 24.1 | 75.0
| GIH | 3.0 | 26.7 | 70.3
| LWK | 11.8 | 39.1 | 49.1
| MEX | 8.6 | 55.2 | 36.2
| MKK | 5.2 | 42.9 | 51.9
| TSI | 6.9 | 52.9 | 40.2
| HapMapRevision=28
}}Source [http://www.nature.com/ng/journal/v38/n10/fig_tab/ng1885_T1.html nature]

Graves' disease or myasthenia gravis	[[rs3129763]](C) + [[rs4639334]](C)

{{PMID Auto GWAS
|PMID=21779181
|Trait=None
|Title=Identification of novel genetic markers associated with clinical phenotypes of systemic sclerosis through a genome-wide association strategy.
|RiskAllele=
|Pval=1E-11
|OR=1.6500
|ORtxt=[1.42-1.91]
|OA=1
}}

{{PMID Auto
|PMID=19176549
|Title=Genome-wide association analysis by lasso penalized logistic regression.
|OA=1
}}

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