ITGB2, integrin subunit beta 2, 3689

N. diseases: 340; N. variants: 31
Disease: Coffin-Siris syndrome ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0265338
Disease: Coffin-Siris syndrome
Coffin-Siris syndrome 		0.010 GeneticVariation disease BEFREE Our data indicate that a common variant of the CD18 gene confers increased risk for CSS and MP, supporting that genetic factors are involved in the etiology and pathogenesis of ANCA-associated systemic vasculitides. 10607485 2000