APP, amyloid beta precursor protein, 351

N. diseases: 485; N. variants: 114
Disease: Familial Alzheimer's disease of early onset ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1200601649
rs1200601649
Entrez Id: 351
Gene Symbol: APP
APP
CUI: C0338445
Disease:
Familial Alzheimer's disease of early onset 		0.010 GeneticVariation BEFREE The G206V mutation in PS1 is probably causal of a case of EOFAD with significant premorbid features. 12112163 2002