{{Rsnum
|rsid=9936833
|Chromosome=16
|position=86369512
|Orientation=plus
|GMAF=0.32
|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 | 9.2 | 55.4 | 35.4
| HCB | 2.3 | 34.1 | 63.6
| JPT | 0.0 | 37.8 | 62.2
| YRI | 14.8 | 41.0 | 44.3
| ASW | 0.0 | 0.0 | 0.0
| CHB | 2.3 | 34.1 | 63.6
| CHD | 0.0 | 0.0 | 0.0
| GIH | 0.0 | 0.0 | 0.0
| LWK | 0.0 | 0.0 | 0.0
| MEX | 0.0 | 0.0 | 0.0
| MKK | 0.0 | 0.0 | 0.0
| TSI | 0.0 | 0.0 | 0.0
| HapMapRevision=28
}}{{PMID Auto
|PMID=22961001
|Title=Common variants at the MHC locus and at chromosome 16q24.1 predispose to Barrett's esophagus
|OA=1
}}

{{PMID Auto
|PMID=23504527
|Title=Barrett associated MHC and FOXF1 variants also increase esophageal carcinoma risk.
}}

{{PMID Auto
|PMID=25164089
|Title=The OSR1 rs12329305 Polymorphism Contributes to the Development of Congenital Malformations in Cases of Stillborn/Neonatal Death
}}
{{on chip | HumanOmni1Quad}}