rs121913507, KIT

N. diseases: 49
Disease: Hypereosinophilia ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Hypereosinophilia
CUI: C0745091
Disease: Hypereosinophilia
0.010 GeneticVariation BEFREE KIT D816V and JAK2 V617F mutations are seen recurrently in hypereosinophilia of unknown significance. 26017288 2015