{{Rsnum
|rsid=12901001
|Gene=AGBL1
|Chromosome=15
|position=86316245
|Orientation=plus
|GMAF=0.461
|Gene_s=AGBL1,OR7E157P
|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 | 9.7 | 40.7 | 49.6
| HCB | 30.7 | 59.9 | 9.5
| JPT | 50.4 | 40.7 | 8.8
| YRI | 30.2 | 49.2 | 20.6
| ASW | 26.3 | 43.9 | 29.8
| CHB | 30.7 | 59.9 | 9.5
| CHD | 38.5 | 45.9 | 15.6
| GIH | 19.8 | 57.4 | 22.8
| LWK | 19.3 | 51.4 | 29.4
| MEX | 20.7 | 60.3 | 19.0
| MKK | 23.2 | 46.5 | 30.3
| TSI | 11.8 | 36.3 | 52.0
| 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=6E-6
  |OR=.15
  |ORtxt=[0.091-0.209] unit increase
  |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}}