{{Rsnum
|rsid=10421768
|Gene=HAMP
|Chromosome=19
|position=35281996
|Orientation=plus
|GMAF=0.1547
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=HAMP
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 60.7 | 36.6 | 2.7
| HCB | 98.5 | 1.5 | 0.0
| JPT | 93.8 | 5.4 | 0.9
| YRI | 73.5 | 23.8 | 2.7
| ASW | 57.9 | 35.1 | 7.0
| CHB | 98.5 | 1.5 | 0.0
| CHD | 0.0 | 0.0 | 0.0
| GIH | 53.5 | 40.6 | 5.9
| LWK | 64.5 | 31.8 | 3.6
| MEX | 55.2 | 39.7 | 5.2
| MKK | 74.4 | 23.1 | 2.6
| TSI | 58.8 | 38.2 | 2.9
| HapMapRevision=28
}}{{PMID Auto
|PMID=19734422
|Title=Association of hepcidin promoter c.-582 A&gt;G variant and iron overload in thalassemia major
|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}}