{{Rsnum
|rsid=296547
|Chromosome=1
|position=200923009
|Orientation=minus
|GMAF=0.4945
|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 | 15.0 | 44.2 | 40.7
| HCB | 38.7 | 46.7 | 14.6
| JPT | 41.1 | 42.0 | 17.0
| YRI | 50.7 | 42.5 | 6.8
| ASW | 45.6 | 40.4 | 14.0
| CHB | 38.7 | 46.7 | 14.6
| CHD | 47.7 | 37.6 | 14.7
| GIH | 19.8 | 49.5 | 30.7
| LWK | 34.5 | 48.2 | 17.3
| MEX | 17.9 | 53.6 | 28.6
| MKK | 34.6 | 53.2 | 12.2
| TSI | 10.8 | 47.1 | 42.2
| HapMapRevision=28
}}
{{PMID Auto GWAS
|PMID=20190752
|Trait=Celiac disease
|Title=Multiple common variants for celiac disease influencing immune gene expression
|RiskAllele=
|Pval=4E-9
|OR=1.12
|ORtxt=[1.09-1.16]
|OA=1
}}

{{PMID|21437271|OA=1
}} Genome-wide interaction-based association analysis identified multiple new susceptibility Loci for common diseases.

{{PMID Auto
|PMID=24871462
|Title=Coeliac disease-associated polymorphisms influence thymic gene expression
}}
{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}