{{Rsnum
|rsid=12928822
|Chromosome=16
|position=11310036
|Orientation=plus
|GMAF=0.09091
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 67.3 | 30.1 | 2.7
| HCB | 89.1 | 10.9 | 0.0
| JPT | 91.2 | 8.8 | 0.0
| YRI | 88.4 | 10.9 | 0.7
| ASW | 87.7 | 12.3 | 0.0
| CHB | 89.1 | 10.9 | 0.0
| CHD | 89.0 | 11.0 | 0.0
| GIH | 87.1 | 12.9 | 0.0
| LWK | 89.1 | 10.9 | 0.0
| MEX | 79.3 | 17.2 | 3.4
| MKK | 95.5 | 4.5 | 0.0
| TSI | 78.4 | 21.6 | 0.0
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=20190752
|Trait=Celiac disease
|Title=Multiple common variants for celiac disease influencing immune gene expression
|RiskAllele=
|Pval=3E-8
|OR=1.16
|ORtxt=[1.10-1.22]
|OA=1
}}

{{PMID|19557189|OA=1
}} Identifying relationships among genomic disease regions: predicting genes at pathogenic SNP associations and rare deletions.

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