Variant: rs63750579 

    present in Gene: APP
    present in Chromosome: 21
    Position on Chromosome: 25891856
    Alleles of this Variant: C/G;T

rs63750579 in APP gene and CEREBRAL AMYLOID ANGIOPATHY, APP-RELATED PMID 11409420 2001 Novel amyloid precursor protein mutation in an Iowa family with dementia and severe cerebral amyloid angiopathy.

PMID 2111584 1990 Mutation of the Alzheimer's disease amyloid gene in hereditary cerebral hemorrhage, Dutch type.

PMID 16178030 2005 A novel AbetaPP mutation exclusively associated with cerebral amyloid angiopathy.

PMID 20298421 2010 EFNS guidelines on the molecular diagnosis of channelopathies, epilepsies, migraine, stroke, and dementias.

PMID 20697050 2010 Hereditary cerebral hemorrhage with amyloidosis associated with the E693K mutation of APP.

PMID 12654973 2003 Hemorrhagic stroke associated with the Iowa amyloid precursor protein mutation.