Variant: rs281865161

present in Gene: APP present in Chromosome: 21 Position on Chromosome: 25897626 Alleles of this Variant: TC/GA

rs281865161 in APP gene and Alzheimer's Disease PMID 23649480 2013 Swedish mutant APP suppresses osteoblast differentiation and causes osteoporotic deficit, which are ameliorated by N-acetyl-L-cysteine.

PMID 21335619 2011 Marked accumulation of 27-hydroxycholesterol in the brains of Alzheimer's patients with the Swedish APP 670/671 mutation.

PMID 8810256 1996 Correlative memory deficits, Abeta elevation, and amyloid plaques in transgenic mice.