{{Rsnum
|rsid=7195303
|Chromosome=16
|position=75133681
|Orientation=plus
|GMAF=0.1111
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=LOC102723987
|Gene_s=LOC102723987
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 79.6 | 19.5 | 0.9
| HCB | 59.1 | 36.5 | 4.4
| JPT | 74.3 | 22.1 | 3.5
| YRI | 89.7 | 10.3 | 0.0
| ASW | 84.2 | 15.8 | 0.0
| CHB | 59.1 | 36.5 | 4.4
| CHD | 50.5 | 46.8 | 2.8
| GIH | 71.3 | 26.7 | 2.0
| LWK | 93.6 | 6.4 | 0.0
| MEX | 93.1 | 5.2 | 1.7
| MKK | 88.2 | 11.8 | 0.0
| TSI | 83.3 | 14.7 | 2.0
| HapMapRevision=28
}}{{PMID Auto GWAS
  |PMID=23665963
  |Trait=Crohn's disease (time to surgery)
  |Title=Multidimensional prognostic risk assessment identifies association between IL12B variation and surgery in Crohn's disease.
  |RiskAllele=G
  |Pval=9E-6
  |OR=2.10
  |ORtxt=[1.5-2.8]
  }}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | FTDNA}}
{{on chip | Illumina Human 1M}}