{{Rsnum
|rsid=4800353
|Chromosome=18
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|position=22074176
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 74.3 | 23.0 | 2.7
| HCB | 65.7 | 32.1 | 2.2
| JPT | 49.6 | 38.9 | 11.5
| YRI | 7.5 | 44.2 | 48.3
| ASW | 19.3 | 36.8 | 43.9
| CHB | 65.7 | 32.1 | 2.2
| CHD | 57.8 | 35.8 | 6.4
| GIH | 64.4 | 32.7 | 3.0
| LWK | 15.5 | 42.7 | 41.8
| MEX | 22.4 | 62.1 | 15.5
| MKK | 26.3 | 49.4 | 24.4
| TSI | 77.5 | 21.6 | 1.0
| 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=T
  |Pval=3E-7
  |OR=1.22
  |ORtxt=[1.14-1.32]
  }}

{{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}}