APP, amyloid beta precursor protein, 351

N. diseases: 485; N. variants: 114
Disease: Amyloidosis ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs529782627
rs529782627
Entrez Id: 351
Gene Symbol: APP
APP
CUI: C0002726
Disease:
Amyloidosis 		0.010 GeneticVariation BEFREE The K16N mutation is located exactly at the α-secretase cleavage site and influences both APP and Aβ. 22514144 2012