{{Rsnum
|rsid=4679904
|Chromosome=3
|position=160623108
|Orientation=plus
|GMAF=0.186
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 52.7 | 36.4 | 10.9
| HCB | 71.6 | 27.6 | 0.7
| JPT | 74.5 | 22.7 | 2.7
| YRI | 85.9 | 13.4 | 0.7
| ASW | 86.0 | 14.0 | 0.0
| CHB | 71.6 | 27.6 | 0.7
| CHD | 72.9 | 24.3 | 2.8
| GIH | 73.5 | 21.4 | 5.1
| LWK | 89.7 | 8.4 | 1.9
| MEX | 59.6 | 29.8 | 10.5
| MKK | 72.1 | 27.3 | 0.6
| TSI | 56.4 | 41.6 | 2.0
| HapMapRevision=28
}}
{{PMID Auto GWAS
|PMID=19458352
|Trait=Primary biliary cirrhosis
|Title=Primary Biliary Cirrhosis Associated with HLA, IL12A, and IL12RB2 Variants
|RiskAllele=G
|Pval=0.000001
|OR=1.38
|ORtxt=[1.21-1.57]
|OA=1
}}

{{GET Evidence
|impact=pathogenic
|qualified_impact=Insufficiently evaluated pathogenic
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs4679904
|overall_frequency_n=24
|overall_frequency_d=128
|overall_frequency=0.1875
|n_genomes=16
|n_genomes_annotated=0
|n_haplomes=20
|n_articles=0
|n_articles_annotated=0
|in_gwas=Y
|autoscore=1
|webscore=N
}}

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