SERPINA3, serpin family A member 3, 12

N. diseases: 229; N. variants: 8
Disease: Complete Trisomy 21 Syndrome ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C4521042
Disease: Complete Trisomy 21 Syndrome
Complete Trisomy 21 Syndrome 		0.010 GeneticVariation disease BEFREE We conclude that unlike the general population, neither PS-1 nor ACT polymorphisms appear to have a similar detrimental effect on dementia in DS.Am.J. Med.Genet.(Neuropsychiatr.Genet.)88:616-620, 1999. 10581479 1999