{{Rsnum
|rsid=7900744
|Gene=IL2RA
|Chromosome=10
|position=6065611
|Orientation=plus
|GMAF=0.2332
|Assembly=GRCh37
|GenomeBuild=37.1
|dbSNPBuild=131
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
}}
{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 61.3 | 33.3 | 5.4
| HCB | 68.2 | 27.3 | 4.5
| JPT | 70.4 | 24.1 | 5.6
| YRI | 23.8 | 50.3 | 25.9
| ASW | 24.6 | 56.1 | 19.3
| CHB | 68.2 | 27.3 | 4.5
| CHD | 0.0 | 0.0 | 0.0
| GIH | 66.0 | 32.0 | 2.0
| LWK | 30.9 | 48.2 | 20.9
| MEX | 87.7 | 12.3 | 0.0
| MKK | 44.2 | 45.5 | 10.3
| TSI | 58.4 | 37.6 | 4.0
| HapMapRevision=28
}}{{Report GE
|PubMed=17371467
|Source=17676041
|AffyProbeset=SNP_A-8468428
|AffyOrientation=same
|AlleleA=A
|AlleleB=G
|onGW5=0
|rsid=7900744
|ancestral=A
|RiskPopulation=UK
|RiskAllele=G
|CaseFreq=
|ControlFreq=
|OddsRatioHet=
|OddsRatioHom=
|OddsRatioAll=1.12
|Disease=Graves' Disease
|DiseaseSymbol=GD
}}

{{PMID|17371467}} a general susceptibility locus for autoimmune disease found via 1896 Graves' disease patients matched to 1822 controls (P = 4.5 x 10(-4)).

rs7900744 is in linkage disequilibrium with a polymorphism that increases susceptibility to Graves' Disease 1.12 times for carriers of the G allele {{PMID|17371467}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}