ITGB3, integrin subunit beta 3, 3690

N. diseases: 260; N. variants: 44
Disease: Echolalia ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0013528
Disease: Echolalia
Echolalia 		0.010 GeneticVariation phenotype BEFREE Although our positive results are not definitive, they suggest small effect associations of the ITGB3 gene with both ASD diagnosis and symptoms of echolalia. 25280596 2014