{{Rsnum
|rsid=10776934
|Chromosome=9
|position=135137855
|Orientation=plus
|GMAF=0.3108
|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 | 53.2 | 41.9 | 4.8
| HCB | 23.1 | 43.6 | 33.3
| JPT | 41.5 | 41.5 | 17.1
| YRI | 71.4 | 23.8 | 4.8
| ASW | 0.0 | 0.0 | 0.0
| CHB | 23.1 | 43.6 | 33.3
| 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=0.000001
|OR=0.2810
|ORtxt=None
}}

{{on chip | FTDNA}}