{{Rsnum
|rsid=9380516
|Chromosome=6
|position=35534425
|Orientation=plus
|GMAF=0.1433
|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 | 69.0 | 28.3 | 2.7
| HCB | 73.0 | 24.8 | 2.2
| JPT | 79.6 | 20.4 | 0.0
| YRI | 76.7 | 21.2 | 2.1
| ASW | 78.9 | 17.5 | 3.5
| CHB | 73.0 | 24.8 | 2.2
| CHD | 69.7 | 28.4 | 1.8
| GIH | 58.4 | 35.6 | 5.9
| LWK | 77.3 | 22.7 | 0.0
| MEX | 91.4 | 8.6 | 0.0
| MKK | 68.6 | 30.1 | 1.3
| TSI | 57.8 | 35.3 | 6.9
| HapMapRevision=28
}}{{PMID Auto GWAS
  |PMID=22841784
  |Trait=Hepatitis C induced liver fibrosis
  |Title=Genome-wide association study identifies variants associated with progression of liver fibrosis from HCV infection.
  |RiskAllele=T
  |Pval=5E-7
  |OR=NR
  |ORtxt=NR
  |OA=1
}}

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