{{Rsnum
|rsid=1869839
|Chromosome=7
|position=114717488
|Orientation=plus
|GMAF=0.2089
|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 | 39.8 | 44.2 | 15.9
| HCB | 69.9 | 27.2 | 2.9
| JPT | 85.8 | 14.2 | 0.0
| YRI | 91.8 | 8.2 | 0.0
| ASW | 85.7 | 14.3 | 0.0
| CHB | 69.9 | 27.2 | 2.9
| CHD | 67.0 | 29.4 | 3.7
| GIH | 57.4 | 35.6 | 6.9
| LWK | 84.5 | 15.5 | 0.0
| MEX | 65.5 | 25.9 | 8.6
| MKK | 90.4 | 8.3 | 1.3
| TSI | 44.6 | 42.6 | 12.9
| HapMapRevision=28
}}{{PMID Auto GWAS
  |PMID=22936669
  |Trait=Crohn's disease
  |Title=A genome-wide association study on a southern European population identifies a new Crohn's disease susceptibility locus at RBX1-EP300.
  |RiskAllele=
  |Pval=7E-6
  |OR=1.20
  |ORtxt=[1.11-1.3]
  }}

{{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}}