{{Rsnum
|rsid=11725957
|Gene=CWH43
|Chromosome=4
|position=49060875
|Orientation=plus
|GMAF=0.01561
|Gene_s=CWH43
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 0.0 | 8.0 | 92.0
| HCB | 0.0 | 0.0 | 0.0
| JPT | 0.0 | 0.0 | 0.0
| YRI | 0.0 | 0.0 | 100.0
| ASW | 0.0 | 0.0 | 0.0
| CHB | 0.0 | 0.0 | 0.0
| CHD | 0.0 | 0.9 | 99.1
| GIH | 0.0 | 2.0 | 98.0
| LWK | 0.0 | 3.6 | 96.4
| MEX | 0.0 | 3.4 | 96.6
| MKK | 0.0 | 0.0 | 0.0
| TSI | 0.0 | 3.9 | 96.1
| 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=0.000008
|OR=0.7270
|ORtxt=None
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | FTDNA}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}