APP, amyloid beta precursor protein, 351

N. diseases: 485; N. variants: 114
Disease: Cortical cataract ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs2096488
rs2096488
Entrez Id: 351
Gene Symbol: APP
APP
CUI: C0271160
Disease:
Cortical cataract 		0.010 GeneticVariation BEFREE Statistical interaction was demonstrated between rs17183619 and APP SNP rs2096488 on CC (P = 0.0015) and CC-THV (P = 0.038). 22984439 2012