{{Rsnum
|rsid=1912785
|Chromosome=3
|position=146684384
|Orientation=plus
|GMAF=0.4669
|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 | 30.1 | 48.7 | 21.2
| HCB | 29.9 | 50.4 | 19.7
| JPT | 21.2 | 48.7 | 30.1
| YRI | 43.2 | 40.4 | 16.4
| ASW | 35.7 | 51.8 | 12.5
| CHB | 29.9 | 50.4 | 19.7
| CHD | 25.7 | 51.4 | 22.9
| GIH | 25.7 | 45.5 | 28.7
| LWK | 22.0 | 51.4 | 26.6
| MEX | 25.9 | 55.2 | 19.0
| MKK | 17.9 | 44.2 | 37.8
| TSI | 28.4 | 53.9 | 17.6
| HapMapRevision=28
}}{{PMID Auto GWAS
  |PMID=22961001
  |Trait=Barrett's esophagus
  |Title=Common variants at the MHC locus and at chromosome 16q24.1 predispose to Barrett's esophagus.
  |RiskAllele=
  |Pval=8E-6
  |OR=.15
  |ORtxt=[0.091-0.209] unit decrease
  |OA=1
}}

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