Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs3851179
rs3851179
0.900 GeneticVariation BEFREE There was no association observed with AD at both rs11136000 CLU (p=0.25) and rs3851179 PICALM (p=0.54). 28558900

2017

dbSNP: rs3851179
rs3851179
0.900 GeneticVariation BEFREE Phosphatidylinositol-binding clathrin assembly protein (PICALM) (rs3851179) has been associated with AD; in particular, the A allele may serve a protective role, while the G allele serves as a strong genetic risk factor. 28549650

2017

dbSNP: rs405509
rs405509
0.900 GeneticVariation BEFREE Rs449647 and rs405509 polymorphisms of <i>APOE</i> gene were not associated with an increase of risk of AD. 28900374

2017

dbSNP: rs405509
rs405509
0.900 GeneticVariation BEFREE These results demonstrate that the rs405509 T/T allele of APOE causes an age-related cognitive decline in non-demented elderly people, possibly by modulating brain network communication efficiency, which may be beneficial for understanding the neural mechanisms of rs405509-related cognitive aging and AD pathogenesis. 27636845

2017

dbSNP: rs63750264
rs63750264
APP
T 0.900 CausalMutation CLINVAR Clinical characterization of an APP mutation (V717I) in five Han Chinese families with early-onset Alzheimer's disease. 27838006

2017

dbSNP: rs63750264
rs63750264
APP
0.900 GeneticVariation BEFREE Alterations in endocytic protein expression with increasing age in the transgenic APP695 V717I London mouse model of amyloid pathology: implications for Alzheimer's disease. 28885485

2017

dbSNP: rs6656401
rs6656401
CR1
0.900 GeneticVariation BEFREE Altogether, five loci (rs6656401 at CR1, rs983392within MS4A6A, rs11218343 at SORL1, rs6733839 at BIN1, and APOE ε4) have been detected to be associated with one or a few established AD-related neuroimaging measures. 26732597

2017

dbSNP: rs744373
rs744373
0.900 GeneticVariation BEFREE The Bridging Integrator 1 Gene Polymorphism rs744373 and the Risk of Alzheimer's Disease in Caucasian and Asian Populations: An Updated Meta-Analysis. 26846281

2017

dbSNP: rs744373
rs744373
0.900 GeneticVariation BEFREE Mutants in rs1800587 of IL-1A, rs1143634 of IL-1B, rs12989701, and rs744373 of BIN1 were significantly associated with AD onset. 26768592

2017

dbSNP: rs744373
rs744373
0.900 GeneticVariation BEFREE The aim of this study was to examine whether the variants of some candidate genes involved in the development of AD, namely BIN1 (rs744373), CLU (rs11136000), CR1 (rs3818361), and PICALM (rs3851179), are related to several disorders of glucose metabolism-gestational diabetes (GDM), T2DM and impaired glucose tolerance (IGT). 28316001

2017

dbSNP: rs75932628
rs75932628
0.900 GeneticVariation BEFREE Shedding is not altered for the R47H-mutated TREM2 protein that confers an increased risk for the development of Alzheimers disease. 28923481

2017

dbSNP: rs11136000
rs11136000
CLU
0.900 GeneticVariation BEFREE Interestingly, the complex communications between resting-state networks were enhanced in aMCI subjects with the CLU rs11136000 CC genotype and were modulated by the degree of memory impairment, suggesting a reconstructed balance of the resting-state networks in these individuals with an elevated risk of AD. 26899953

2016

dbSNP: rs2075650
rs2075650
0.900 GeneticVariation BEFREE Collectively, our analysis shows TOMM40 rs2075650 polymorphism is associated with AD susceptibility in Asian, Caucasian, and mixed populations. 27328316

2016

dbSNP: rs2075650
rs2075650
0.900 GeneticVariation BEFREE Similarly, our evidence suggested that allele A of TOMM40 rs2075650 polymorphism was a risk factor for AD (OR=2.87, 95% CI: 2.46-3.34, P value <0.001). 26795201

2016

dbSNP: rs2075650
rs2075650
0.900 GeneticVariation BEFREE Both methods' results showed two identical significant SNPs associated with the A β-42 levels in CSF (rs2075650 at intron region TOMM40 with p-value ≥ 1 × 10-16 and rs439401 in the intergenic region of LOC100129500 and APOC1 with p-value ≥ 1 × 10-9) and highlighted APOC1 and TOMM40, which are well-known genes previously associated with AD. 26576771

2016

dbSNP: rs2075650
rs2075650
0.900 GeneticVariation BEFREE We conclude that rs2075650 in TOMM40 gene may increase the risk of Alzheimer disease. 26572157

2016

dbSNP: rs2075650
rs2075650
0.900 GeneticVariation GWASCAT Genetic risk factors for the posterior cortical atrophy variant of Alzheimer's disease. 26993346

2016

dbSNP: rs2373115
rs2373115
0.900 GeneticVariation BEFREE There was no significant association between SNPs of GAB2 rs2373115 (G > T) and PICALM rs541458 (C > T) and AD. 26611835

2016

dbSNP: rs3764650
rs3764650
0.900 GeneticVariation BEFREE A comprehensive literature search for studies involving the association between gene polymorphisms and AD was performed, and we finally selected 3 genes (4 polymorphisms) for the meta-analysis: ABCA7 (rs3764650), CD33 (rs3865444), and TOMM40 (rs157580, rs2075650). 26795201

2016

dbSNP: rs3851179
rs3851179
0.900 GeneticVariation BEFREE Re: "PICALM Gene rs3851179 Polymorphism Contributes to Alzheimer's Disease in an Asian Population". 26972434

2016

dbSNP: rs3851179
rs3851179
0.900 GeneticVariation BEFREE The allele T of rs38</span>51179 in PICALM was associated with a 13 % increase in the risk of AD. 26611835

2016

dbSNP: rs3851179
rs3851179
0.900 GeneticVariation BEFREE The association between rs3851179 (PICALM), rs744373 (BIN1), and AD was further confirmed by meta-analysis of Asian populations. 25452228

2016

dbSNP: rs3865444
rs3865444
0.900 GeneticVariation BEFREE Alleles A of CD33 rs3865444 and A of TOMM40 rs157580 were both protective factors for AD onset (OR=0.94, 95% CI: 0.90-0.98, P value=0.003; OR=0.62, 95% CI: 0.57-0.66, P value <0.001). 26795201

2016

dbSNP: rs405509
rs405509
0.900 GeneticVariation BEFREE Evidence demonstrates that the T allele of the single-nucleotide polymorphism rs405509 in the apolipoprotein E (APOE) promoter is a risk factor for Alzheimer's disease. 27259692

2016

dbSNP: rs405509
rs405509
0.900 GeneticVariation BEFREE Evidence demonstrates that the T allele of the single-nucleotide polymorphism rs405509 as the apolipoprotein E (APOE) promoter is a risk factor for Alzheimer's disease (AD). 26825091

2016