{{Rsnum
|rsid=7632500
|Chromosome=3
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|position=168007561
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 90.3 | 9.7 | 0.0
| HCB | 77.2 | 22.1 | 0.7
| JPT | 82.3 | 15.0 | 2.7
| YRI | 25.2 | 45.6 | 29.3
| ASW | 24.6 | 54.4 | 21.1
| CHB | 77.2 | 22.1 | 0.7
| CHD | 82.6 | 15.6 | 1.8
| GIH | 92.1 | 7.9 | 0.0
| LWK | 33.9 | 47.7 | 18.3
| MEX | 72.4 | 24.1 | 3.4
| MKK | 30.8 | 53.2 | 16.0
| TSI | 87.3 | 12.7 | 0.0
| 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=C
  |Pval=1E-6
  |OR=1.37
  |ORtxt=[1.21-1.55]
  }}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}