Gene: FCGR3B ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 2215
Gene Symbol: FCGR3B
FCGR3B 		0.010 Biomarker disease BEFREE We conclude that PMN-FcRIII deficiency is a rare phenomenon that can lead to CD16 alloimmunization and thus cause NAIN. 1532916 1992