{{Rsnum
|rsid=7800244
|Chromosome=7
|position=47740371
|Orientation=plus
|GMAF=0.157
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
}}{{ population diversity
| geno1=(G;G)
| geno2=(G;T)
| geno3=(T;T)
| CEU | 62.8 | 34.5 | 2.7
| HCB | 65.4 | 32.4 | 2.2
| JPT | 66.1 | 28.6 | 5.4
| YRI | 91.2 | 8.8 | 0.0
| ASW | 75.4 | 24.6 | 0.0
| CHB | 65.4 | 32.4 | 2.2
| CHD | 65.1 | 33.9 | 0.9
| GIH | 68.3 | 30.7 | 1.0
| LWK | 90.8 | 9.2 | 0.0
| MEX | 74.1 | 22.4 | 3.4
| MKK | 69.7 | 29.7 | 0.6
| TSI | 68.6 | 27.5 | 3.9
| 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=3E-6
  |OR=NR
  |ORtxt=NR
  |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}}