Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs77375493
rs77375493
CUI: C0745091
Disease: Hypereosinophilia
Hypereosinophilia
0.010 GeneticVariation BEFREE KIT D816V and JAK2 V617F mutations are seen recurrently in hypereosinophilia of unknown significance. 26017288

2015