rs1402522059, CAT

N. diseases: 1
Disease: Hemochromatosis ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Hemochromatosis
CUI: C0018995
Disease: Hemochromatosis
0.010 GeneticVariation BEFREE Eight control subjects homozygous for mutation His63Asp showed no biochemical or clinical evidence of haemochromatosis indicating that this variant is not directly responsible for haemochromatosis. 9382962 1997