POU2F1, POU class 2 homeobox 1, 5451

N. diseases: 115; N. variants: 7
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0019025
Disease: Hemoglobin F Disease
Hemoglobin F Disease
0.010 GeneticVariation disease BEFREE Binding of OTF-1 to this region is reduced by a mutation at -175 associated with a form of non-deletion hereditary persistence of fetal hemoglobin. 2336386 1990