APP, amyloid beta precursor protein, 351

N. diseases: 485; N. variants: 114
Disease: Dementia ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs63750264
rs63750264
Entrez Id: 351
Gene Symbol: APP
APP
CUI: C0497327
Disease:
Dementia 		0.010 GeneticVariation BEFREE A novel mutation in the APPgene (V717L) has been found in a family with a history of dementia, beginning in the mid to late 30s. 10867787 2000