Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs63749810
rs63749810
Entrez Id: 351
Gene Symbol: APP
APP
CUI: C1843013
Disease:
Alzheimer disease, familial, type 3
0.010 GeneticVariation BEFREE The reported APP-D694N iPSC line may be used to model and study human AD pathology in vitro. 31004935 2019