{{Rsnum
|rsid=11103429
|Chromosome=9
|position=134614732
|Orientation=plus
|GMAF=0.08402
|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 | 92.9 | 6.2 | 0.9
| HCB | 92.0 | 8.0 | 0.0
| JPT | 94.7 | 5.3 | 0.0
| YRI | 63.3 | 34.7 | 2.0
| ASW | 68.4 | 26.3 | 5.3
| CHB | 92.0 | 8.0 | 0.0
| CHD | 92.7 | 6.4 | 0.9
| GIH | 86.1 | 13.9 | 0.0
| LWK | 68.8 | 30.3 | 0.9
| MEX | 82.8 | 15.5 | 1.7
| MKK | 71.2 | 28.2 | 0.6
| TSI | 89.2 | 10.8 | 0.0
| HapMapRevision=28
}}{{PMID Auto GWAS
  |PMID=23665963
  |Trait=Crohn's disease (need for surgery)
  |Title=Multidimensional prognostic risk assessment identifies association between IL12B variation and surgery in Crohn's disease.
  |RiskAllele=G
  |Pval=6E-6
  |OR=3.60
  |ORtxt=[2.10-6.30]
  }}

{{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}}