MYB, MYB proto-oncogene, transcription factor, 4602

N. diseases: 206; N. variants: 30
Disease: Eosinophilia ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0014457
Disease: Eosinophilia
Eosinophilia 		0.020 GeneticVariation disease BEFREE SNPs within MYB itself confer susceptibility to eosinophilia and asthma. 23606399 2013
CUI: C0014457
Disease: Eosinophilia
Eosinophilia 		0.020 GeneticVariation disease BEFREE We recruited 284 patients with NP in four participating hospitals in Belgium and 427 healthy controls, and genotyped 10 SNPs affecting eosinophilia (rs1420101 in IL1RL1, rs12619285 in IKZF2, rs4431128 in GATA2, rs4143832 in IL5, rs3184504 in SH2B3, rs2416257 in WDR36, rs2269426 in MHC, rs9494145 in MYB, rs748065 in GFRA2, and rs3939286 in IL33) using MALDI-TOF. 19860791 2010