rs1081105
|
|
C |
0.700 |
GeneticVariation |
GWASCAT |
Genome-wide meta-analysis identifies new loci and functional pathways influencing Alzheimer's disease risk.
|
30617256 |
2019 |
rs1081105
|
|
|
0.700 |
GeneticVariation |
GWASCAT |
GWAS on family history of Alzheimer's disease.
|
29777097 |
2018 |
rs11542041
|
|
|
0.010 |
GeneticVariation |
BEFREE |
ApoE single nucleotide polymorphisms (SNPs) Cys112Arg (Epsilon-4), and Arg158Cys (Epsilon-2) have been implicated in cardiovascular and Alzheimer's disease, but their role in colorectal cancer (CRC) has not been extensively studied.
|
19455140 |
2009 |
rs1167428194
|
|
|
0.010 |
GeneticVariation |
BEFREE |
Nonetheless, the AD associated intronic haplotype is linked to the 338A variant of known ECE1b promoter variant, 338C>A (rs213045).
|
22693153 |
2012 |
rs1233347077
|
|
|
0.020 |
GeneticVariation |
BEFREE |
IL-6 (-174 C/G) polymorphism is not a risk factor for late onset AD in a Polish population.
|
21225514 |
2011 |
rs1233347077
|
|
|
0.020 |
GeneticVariation |
BEFREE |
Furthermore, there was no evidence of linkage disequilibrium between the VNTR and -174G/C polymorphisms, not supporting a previous reported additive effect of both IL-6 polymorphisms on AD risk.
|
19897004 |
2010 |
rs1270059098
|
|
|
0.010 |
GeneticVariation |
BEFREE |
In conclusion, our meta-analysis demonstrates that 5HT2A C10T, but not 5HTTLPR (L/S), might increase risk for AD.
|
29599928 |
2018 |
rs1424027593
|
|
|
0.010 |
GeneticVariation |
BEFREE |
Association between the ABCG2 C421A polymorphism and Alzheimer's disease.
|
23827224 |
2013 |
rs1438607869
|
|
|
0.010 |
GeneticVariation |
BEFREE |
These results suggested that PEMT G523A is associated with AD and that the A allele is an APOE ε4-independent risk factor for AD among Han Chinese women.
|
21881829 |
2012 |
rs1440976751
|
|
|
0.020 |
GeneticVariation |
BEFREE |
Recent studies have reported a genetic association between the 73 G/A polymorphism within exon 1 of the cystatin C gene and Alzheimer's disease (AD) with conflicting results.
|
16188386 |
2006 |
rs1440976751
|
|
|
0.020 |
GeneticVariation |
BEFREE |
The G73A polymorphism of the CST3 genemay be associated with AD development.
|
18408364 |
2008 |
rs199768005
|
|
|
0.010 |
GeneticVariation |
BEFREE |
ApoE variant p.V236E is associated with markedly reduced risk of Alzheimer's disease.
|
24607147 |
2014 |
rs405509
|
|
|
0.900 |
GeneticVariation |
GWASDB |
Dementia revealed: novel chromosome 6 locus for late-onset Alzheimer disease provides genetic evidence for folate-pathway abnormalities.
|
20885792 |
2010 |
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 |
rs405509
|
|
|
0.900 |
GeneticVariation |
BEFREE |
Education, sex, and the APOE-rs405509 variant are associated with Alzheimer's disease and cognitive performance.
|
31100889 |
2019 |
rs405509
|
|
|
0.900 |
GeneticVariation |
GWASDB |
Common variants at MS4A4/MS4A6E, CD2AP, CD33 and EPHA1 are associated with late-onset Alzheimer's disease.
|
21460841 |
2011 |
rs405509
|
|
|
0.900 |
GeneticVariation |
BEFREE |
This association is biologically plausible as SNP rs405509 was shown to modify protein binding and transcriptional activity of the APOE protein in vitro and is in linkage disequilibrium with key known variants defining the e2, e3, and e4 alleles that modify risk of atherosclerosis, Alzheimer's disease risk, and progression to AIDS.
|
19808960 |
2009 |
rs405509
|
|
|
0.900 |
GeneticVariation |
BEFREE |
In the presented study, we investigated the association between -491 A/T (rs449647), -427C/T, (rs769446) and -219 T/G (rs405509) single nucleotide polymorphisms (SNPs) of APOE gene and AD risk in the Polish population.
|
29990559 |
2018 |
rs405509
|
|
|
0.900 |
GeneticVariation |
GWASDB |
Genome-wide association of familial late-onset Alzheimer's disease replicates BIN1 and CLU and nominates CUGBP2 in interaction with APOE.
|
21379329 |
2011 |
rs405509
|
|
T |
0.900 |
GeneticVariation |
GWASDB |
Overrepresentation of glutamate signaling in Alzheimer's disease: network-based pathway enrichment using meta-analysis of genome-wide association studies.
|
24755620 |
2014 |
rs405509
|
|
|
0.900 |
GeneticVariation |
GWASDB |
Genome-wide association study of Alzheimer's disease with psychotic symptoms.
|
22005930 |
2012 |
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 |
rs405509
|
|
|
0.900 |
GeneticVariation |
GWASDB |
Genome-wide association study identifies variants at CLU and CR1 associated with Alzheimer's disease.
|
19734903 |
2009 |
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 |
rs405509
|
|
|
0.900 |
GeneticVariation |
BEFREE |
The single nucleotide polymorphisms (SNPs) rs449647, rs769446 and rs405509 in the promoter region of the APOE gene have been variously suggested to be epsilon 4-independent risk factors for Alzheimer's disease (AD).
|
19172988 |
2009 |