SMAP2, small ArfGAP2, 64744

N. diseases: 3; N. variants: 0
Disease: aspirin intolerance ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0004059
Disease: aspirin intolerance
aspirin intolerance 		0.010 Biomarker phenotype BEFREE Our findings suggest that SMAP1L might be a susceptible gene to AIA, providing a new strategy for the control of aspirin intolerance. 20831471 2010