{{Rsnum
|rsid=2243123
|Gene=IL12A
|Chromosome=3
|position=159991864
|Orientation=plus
|GMAF=0.1979
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=IL12A,IL12A-AS1
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 9.7 | 38.9 | 51.3
| HCB | 0.0 | 21.9 | 78.1
| JPT | 1.8 | 14.2 | 84.1
| YRI | 1.4 | 27.2 | 71.4
| ASW | 0.0 | 19.3 | 80.7
| CHB | 0.0 | 21.9 | 78.1
| CHD | 0.9 | 12.0 | 87.0
| GIH | 2.0 | 17.8 | 80.2
| LWK | 0.0 | 15.5 | 84.5
| MEX | 12.1 | 43.1 | 44.8
| MKK | 1.9 | 15.4 | 82.7
| TSI | 4.9 | 36.3 | 58.8
| HapMapRevision=28
}}{{PMID Auto
|PMID=21606320
|Title=Genetic Associations with Sporadic Neuroendocrine Tumor Risk
|OA=1
}}

{{PMID Auto
|PMID=18671862
|Title=Polymorphisms in IL12A and cockroach allergy in children with asthma.
|OA=1
}}

{{PMID Auto
|PMID=21044109
|Title=Association study of interleukin-12A gene polymorphisms with Graves' disease in two Chinese populations.
}}

{{PMID Auto
|PMID=22515181
|Title=Interleukin-12: clinical usage and molecular markers of cancer susceptibility.
}}

{{PMID Auto GWAS
  |PMID=21833088
  |Trait=Multiple sclerosis
  |Title=Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis.
  |RiskAllele=G
  |Pval=7E-6
  |OR=1.08
  |ORtxt=[1.06-1.1]
  |OA=1
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | FTDNA}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}