APP, amyloid beta precursor protein, 351

N. diseases: 485; N. variants: 114
Disease: Parkinson Disease ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs466448
rs466448
Entrez Id: 351
Gene Symbol: APP
APP
CUI: C0030567
Disease:
Parkinson Disease 		0.010 GeneticVariation BEFREE Significant correlation with CSF Aβ42 levels in PD was observed for two SNPs, (APP rs466448 and APH1B rs2068143). 25808939 2015