Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs63750215
rs63750215
0.100 GeneticVariation BEFREE We describe a new mutation causing Alzheimer's disease (AD) in presenilin-1 (N135D) that is at the homologous site to the presenilin 2 mutation (N141I) in Volga German kindreds. 9225696

1997

dbSNP: rs778936527
rs778936527
0.010 GeneticVariation BEFREE We found the mutations, G384A, E280A in two FAD and H163R in one sporadic AD patient, and no N1411 or M239V mutation in PS-2 gene, and no mutation in exons 16 and 17 in amyloid precursor protein (APP) gene. 8945747

1996

dbSNP: rs8383
rs8383
0.010 GeneticVariation BEFREE Our analysis supports the hypothesis that the PSEN2 rs8383 polymorphism is associated with an enlarged risk of sporadic AD. 22580083

2012