rs779021719, HAMP

N. diseases: 5
Disease: Hepatic siderosis ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Hepatic siderosis
CUI: C0948120
Disease: Hepatic siderosis
0.010 GeneticVariation BEFREE Individuals homozygous for the A1AT Z-allele with environmental or genetic risk factors such as steatosis or heterozygosity for the HAMP non-sense mutation p.Arg59* presented with severe hepatic siderosis. 26310624 2015