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: C2751536
Disease:
CEREBRAL AMYLOID ANGIOPATHY, APP-RELATED
0.800 GeneticVariation UNIPROT
dbSNP: rs63749810
rs63749810
Entrez Id: 351
Gene Symbol: APP
APP
CUI: C2751536
Disease:
CEREBRAL AMYLOID ANGIOPATHY, APP-RELATED
T 0.800 CausalMutation CLINVAR