Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs3736187
rs3736187
MME
0.020 GeneticVariation BEFREE This meta-analysis indicates that rs3736187 (A/G) polymorphisms may be a potential beneficial single nucleotide polymorphism (SNP), which are associated with a decreased risk in AD. 25125048

2014

dbSNP: rs989692
rs989692
MME
0.020 GeneticVariation BEFREE The pooled odds ratio (OR) and confidence interval (CI) suggested that rs989692 polymorphisms were not associated with AD based on the current published studies (C vs. T, OR = 1.01, 95% CI = 0.85-1.19; CC+TT vs. CT, OR = 0.89, 95% CI = 0.78-1.01). 25125048

2014

dbSNP: rs3736187
rs3736187
MME
0.020 GeneticVariation BEFREE Two SNPs, rs989692 and rs3736187, had significantly different allelic and genotypic frequencies (uncorrected p = 0.01) between the AD and the control subjects and haplotype analysis showed significant association between AD and NEP polymorphisms. 15548496

2004

dbSNP: rs989692
rs989692
MME
0.020 GeneticVariation BEFREE Two SNPs, rs989692 and rs3736187, had significantly different allelic and genotypic frequencies (uncorrected p = 0.01) between the AD and the control subjects and haplotype analysis showed significant association between AD and NEP polymorphisms. 15548496

2004

dbSNP: rs1816558
rs1816558
MME
0.010 GeneticVariation BEFREE SNP rs1816558 of NEP was found to be significantly associated with AD after adjustment for ε4 allele of the apolipoprotein E gene (APOEε4) and the Bonferroni correction. 26362309

2016

dbSNP: rs1327722411
rs1327722411
MME
0.010 GeneticVariation BEFREE Five point mutations within the amyloid beta-protein (Abeta) sequence of the APP gene are associated with hereditary diseases which are similar or identical to Alzheimer's disease and encode: the A21G (Flemish), E22G (Arctic), E22K (Italian), E22Q (Dutch) and the D23N (Iowa) amino acid substitutions. 18602473

2008

dbSNP: rs1836915
rs1836915
MME
0.010 GeneticVariation BEFREE SNP rs1836915, in linkage disequilibrium block 2, showed the greatest extent of genotypic association with AD (p=0.0076). 17928142

2007