{{Rsnum
|rsid=11242704
|Chromosome=6
|position=1535763
|Orientation=plus
|GMAF=0.4454
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=LOC102723958
|Gene_s=LOC102723958
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 44.2 | 47.8 | 8.0
| HCB | 24.1 | 48.9 | 27.0
| JPT | 35.4 | 47.8 | 16.8
| YRI | 4.1 | 27.2 | 68.7
| ASW | 14.0 | 49.1 | 36.8
| CHB | 24.1 | 48.9 | 27.0
| CHD | 25.7 | 49.5 | 24.8
| GIH | 46.5 | 42.6 | 10.9
| LWK | 12.7 | 49.1 | 38.2
| MEX | 50.0 | 44.8 | 5.2
| MKK | 14.1 | 44.2 | 41.7
| TSI | 49.0 | 34.3 | 16.7
| 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=G
|Pval=0.000005
|OR=0.2570
|ORtxt=None
}}

{{on chip | Affy GenomeWide 6}}
{{on chip | FTDNA}}
{{on chip | HumanOmni1Quad}}