{{Rsnum
|rsid=2178146
|Chromosome=16
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|position=86430089
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 33.6 | 46.0 | 20.4
| HCB | 59.6 | 37.5 | 2.9
| JPT | 55.8 | 39.8 | 4.4
| YRI | 100.0 | 0.0 | 0.0
| ASW | 91.2 | 8.8 | 0.0
| CHB | 59.6 | 37.5 | 2.9
| CHD | 59.6 | 37.6 | 2.8
| GIH | 58.4 | 35.6 | 5.9
| LWK | 0.0 | 0.0 | 0.0
| MEX | 39.7 | 41.4 | 19.0
| MKK | 96.8 | 3.2 | 0.0
| TSI | 48.0 | 39.2 | 12.7
| HapMapRevision=28
}}{{PMID Auto GWAS
  |PMID=24121790
  |Trait=Digestive system disease (Barrett's esophagus and esophageal adenocarcinoma combined)
  |Title=A genome-wide association study identifies new susceptibility loci for esophageal adenocarcinoma and Barrett's esophagus.
  |RiskAllele=A
  |Pval=1E-6
  |OR=1.14
  |ORtxt=[1.09-1.2]
  }}

{{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}}