Source: CLINVAR

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs281865161
rs281865161
APP
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease 		GA 0.700 CausalMutation CLINVAR Swedish mutant APP suppresses osteoblast differentiation and causes osteoporotic deficit, which are ameliorated by N-acetyl-L-cysteine. 23649480

2013
dbSNP: rs281865161
rs281865161
APP
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease 		GA 0.700 CausalMutation CLINVAR Marked accumulation of 27-hydroxycholesterol in the brains of Alzheimer's patients with the Swedish APP 670/671 mutation. 21335619

2011
dbSNP: rs281865161
rs281865161
APP
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease 		GA 0.700 CausalMutation CLINVAR Correlative memory deficits, Abeta elevation, and amyloid plaques in transgenic mice. 8810256

1996