Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs63750579
rs63750579
APP
0.800 GeneticVariation UNIPROT Hereditary cerebral hemorrhage with amyloidosis associated with the E693K mutation of APP. 20697050

2010
dbSNP: rs63750579
rs63750579
APP
0.800 GeneticVariation UNIPROT EFNS guidelines on the molecular diagnosis of channelopathies, epilepsies, migraine, stroke, and dementias. 20298421

2010
dbSNP: rs63750579
rs63750579
APP
0.800 GeneticVariation UNIPROT A novel AbetaPP mutation exclusively associated with cerebral amyloid angiopathy. 16178030

2005
dbSNP: rs63750579
rs63750579
APP
0.800 GeneticVariation UNIPROT Hemorrhagic stroke associated with the Iowa amyloid precursor protein mutation. 12654973

2003
dbSNP: rs63750579
rs63750579
APP
0.800 GeneticVariation UNIPROT Novel amyloid precursor protein mutation in an Iowa family with dementia and severe cerebral amyloid angiopathy. 11409420

2001
dbSNP: rs63750579
rs63750579
APP
0.800 GeneticVariation UNIPROT Mutation of the Alzheimer's disease amyloid gene in hereditary cerebral hemorrhage, Dutch type. 2111584

1990
dbSNP: rs63749810
rs63749810
APP
0.800 GeneticVariation UNIPROT

dbSNP: rs63749810
rs63749810
APP
T 0.800 CausalMutation CLINVAR

dbSNP: rs63750579
rs63750579
APP
T 0.800 CausalMutation CLINVAR

dbSNP: rs63750579
rs63750579
APP
G 0.800 CausalMutation CLINVAR

dbSNP: rs63750671
rs63750671
APP
C 0.700 CausalMutation CLINVAR

dbSNP: rs63750921
rs63750921
APP
0.700 GeneticVariation UNIPROT

dbSNP: rs63751039
rs63751039
APP
C 0.700 CausalMutation CLINVAR