{{Rsnum
|rsid=16851720
|Gene=RNF7
|Chromosome=3
|position=141744456
|Orientation=plus
|GMAF=0.1846
|Gene_s=RNF7
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;C)
| geno3=(C;C)
| CEU | 61.1 | 33.6 | 5.3
| HCB | 91.2 | 8.8 | 0.0
| JPT | 81.4 | 17.7 | 0.9
| YRI | 56.5 | 34.7 | 8.8
| ASW | 52.6 | 38.6 | 8.8
| CHB | 91.2 | 8.8 | 0.0
| CHD | 85.3 | 14.7 | 0.0
| GIH | 69.0 | 29.0 | 2.0
| LWK | 50.0 | 37.3 | 12.7
| MEX | 79.3 | 17.2 | 3.4
| MKK | 57.4 | 38.1 | 4.5
| TSI | 65.7 | 28.4 | 5.9
| 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=C
  |Pval=9E-9
  |OR=NR
  |ORtxt=NR
  |OA=1
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}