{{Rsnum
|rsid=12527818
|Chromosome=6
|position=93201401
|Orientation=plus
|GMAF=0.2842
|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 | 28.3 | 61.7
| HCB | 17.1 | 41.5 | 41.5
| JPT | 23.8 | 42.9 | 33.3
| YRI | 0.0 | 6.8 | 93.2
| ASW | 0.0 | 0.0 | 0.0
| CHB | 17.1 | 41.5 | 41.5
| CHD | 0.0 | 0.0 | 0.0
| GIH | 0.0 | 0.0 | 0.0
| LWK | 0.0 | 0.0 | 0.0
| MEX | 0.0 | 0.0 | 0.0
| MKK | 0.0 | 0.0 | 0.0
| TSI | 0.0 | 0.0 | 0.0
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=22095909
|Trait=None
|Title=Serum ferritin levels are associated with a distinct phenotype of chronic hepatitis C poorly responding to pegylated interferon-alpha and ribavirin therapy.
|RiskAllele=T
|Pval=0.000007
|OR=0.2740
|ORtxt=None
}}