{{Rsnum
|rsid=9275390
|Chromosome=6
|position=32701379
|Orientation=plus
|GMAF=0.3136
|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 | 10.0 | 43.6 | 46.4
| HCB | 5.2 | 37.8 | 57.0
| JPT | 12.5 | 43.8 | 43.8
| YRI | 9.7 | 38.6 | 51.7
| ASW | 12.3 | 42.1 | 45.6
| CHB | 5.2 | 37.8 | 57.0
| CHD | 4.6 | 37.0 | 58.3
| GIH | 4.0 | 32.7 | 63.4
| LWK | 13.8 | 40.4 | 45.9
| MEX | 17.5 | 49.1 | 33.3
| MKK | 8.4 | 38.7 | 52.9
| TSI | 2.0 | 36.6 | 61.4
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=21779181
|Trait=None
|Title=Identification of novel genetic markers associated with clinical phenotypes of systemic sclerosis through a genome-wide association strategy.
|RiskAllele=
|Pval=1E-7
|OR=1.6100
|ORtxt=[1.35-1.92]
|OA=1
}}

{{PMID|19458352|OA=1
}} Primary biliary cirrhosis associated with HLA, IL12A, and IL12RB2 variants.

{{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}}