{{Rsnum
|rsid=3129860
|Chromosome=6
|position=32433302
|Orientation=plus
|GMAF=0.09734
|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 | 4.5 | 29.5 | 66.1
| HCB | 1.5 | 21.5 | 77.0
| JPT | 4.5 | 34.8 | 60.7
| YRI | 0.0 | 9.0 | 91.0
| ASW | 0.0 | 7.0 | 93.0
| CHB | 1.5 | 21.5 | 77.0
| CHD | 0.0 | 13.0 | 87.0
| GIH | 1.0 | 18.0 | 81.0
| LWK | 0.9 | 9.2 | 89.9
| MEX | 0.0 | 17.2 | 82.8
| MKK | 0.6 | 5.8 | 93.6
| TSI | 2.0 | 14.9 | 83.2
| HapMapRevision=28
}}{{PMID Auto GWAS
  |PMID=23321320
  |Trait=Hepatitis C induced liver cirrhosis
  |Title=A genome-wide association study of HCV-induced liver cirrhosis in the Japanese population identifies novel susceptibility loci at the MHC region.
  |RiskAllele=A
  |Pval=1E-9
  |OR=1.36
  |ORtxt=[1.22-1.49]
  }}

{{PMID Auto
|PMID=20405052
|Title=The effect of single nucleotide polymorphisms from genome wide association studies in multiple sclerosis on gene expression.
|OA=1
}}

{{PMID Auto
|PMID=21379322
|Title=Risk alleles for systemic lupus erythematosus in a large case-control collection and associations with clinical subphenotypes.
|OA=1
}}

{{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}}