{{Rsnum
|rsid=4820425
|Chromosome=22
|position=41035338
|Orientation=plus
|GMAF=0.2383
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;C)
| geno3=(C;C)
| CEU | 10.6 | 45.1 | 44.2
| HCB | 1.5 | 18.2 | 80.3
| JPT | 0.0 | 1.8 | 98.2
| YRI | 0.7 | 15.6 | 83.7
| ASW | 1.8 | 35.1 | 63.2
| CHB | 1.5 | 18.2 | 80.3
| CHD | 0.9 | 20.2 | 78.9
| GIH | 8.9 | 55.4 | 35.6
| LWK | 0.9 | 13.6 | 85.5
| MEX | 39.7 | 48.3 | 12.1
| MKK | 0.6 | 23.1 | 76.3
| TSI | 4.9 | 41.2 | 53.9
| 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=A
  |Pval=3E-8
  |OR=1.27
  |ORtxt=[1.17-1.38]
  }}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA}}
{{on chip | Illumina Human 1M}}