APP, amyloid beta precursor protein, 351

N. diseases: 485; N. variants: 114
Disease: Impaired cognition ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1800557
rs1800557
Entrez Id: 351
Gene Symbol: APP
APP
CUI: C0338656
Disease:
Impaired cognition 		0.010 GeneticVariation BEFREE We recently reported an alanine to valine mutation in codon 713 in a single case of chronic familial schizophrenia with cognitive deficits. 8049900 1994