GCG, glucagon, 2641

N. diseases: 441; N. variants: 10
Disease: Thalassemia ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0039730
Disease: Thalassemia
Thalassemia 		0.010 GeneticVariation group BEFREE Mutation analysis identified the Hb Raleigh (β1[NA1]Val → Ala [GTG → GCG]) mutation in combination with an α(+)-thalassaemia, a hitherto undescribed association. 22829696 2012