Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs4718789
rs4718789
T 0.700 GeneticVariation GWASCAT Genome-wide association study of HIV-associated neurocognitive disorder (HAND): A CHARTER group study. 28447399

2017

dbSNP: rs4978818
rs4978818
C 0.700 GeneticVariation GWASCAT Genome-wide association study of HIV-associated neurocognitive disorder (HAND): A CHARTER group study. 28447399

2017

dbSNP: rs6265
rs6265
0.070 GeneticVariation BEFREE Impact of APOE and BDNF Val66Met Gene Polymorphisms on Cognitive Functions in Patients with Amnestic Mild Cognitive Impairment. 31771052

2020

dbSNP: rs6265
rs6265
0.070 GeneticVariation BEFREE A total of 1,081 adults without dementia (375 healthy subjects and 706 individuals with mild cognitive impairment) were recruited from the Alzheimer's Disease Neuroimaging Initiative (ADNI) to test the influence of BDNF Val66Met polymorphism on cognitive impairment, brain structure atrophy, and change in the levels of CSF biomarkers. 30775992

2019

dbSNP: rs6265
rs6265
0.070 GeneticVariation BEFREE To compare the results of neuropsychological tests, evoked potentials N200 and P300 and polymorphisms of ApoE and BDNF rs6265 between patients with normal cognition and those with mild cognitive impairment (MCI) and Alzheimer's dementia (AD). 28833437

2018

dbSNP: rs6265
rs6265
0.070 GeneticVariation BEFREE Physical exercise improves peripheral BDNF levels and cognitive functions in mild cognitive impairment elderly with different bdnf Val66Met genotypes. 25062900

2015

dbSNP: rs6265
rs6265
0.070 GeneticVariation BEFREE Association between BDNF polymorphism (Val66Met) and executive function in patients with amnestic mild cognitive impairment or mild Alzheimer disease. 22699449

2012

dbSNP: rs6265
rs6265
0.070 GeneticVariation BEFREE Although Val66Met polymorphisms were not associated with the cross-sectional diagnoses of MCI or AD, the presence of Met-BDNF allele was associated with a higher risk of disease-progression in patients with MCI (OR=3.0 CI(95%) [1.2-7.8], P=0.02). 20491609

2010

dbSNP: rs6265
rs6265
0.070 GeneticVariation BEFREE The BDNF Val66Met polymorphism was not associated with serum BDNF or cognitive function in aMCI patients. 18505307

2008

dbSNP: rs759834365
rs759834365
0.060 GeneticVariation BEFREE Impact of APOE and BDNF Val66Met Gene Polymorphisms on Cognitive Functions in Patients with Amnestic Mild Cognitive Impairment. 31771052

2020

dbSNP: rs759834365
rs759834365
0.060 GeneticVariation BEFREE A total of 1,081 adults without dementia (375 healthy subjects and 706 individuals with mild cognitive impairment) were recruited from the Alzheimer's Disease Neuroimaging Initiative (ADNI) to test the influence of BDNF Val66Met polymorphism on cognitive impairment, brain structure atrophy, and change in the levels of CSF biomarkers. 30775992

2019

dbSNP: rs759834365
rs759834365
0.060 GeneticVariation BEFREE Physical exercise improves peripheral BDNF levels and cognitive functions in mild cognitive impairment elderly with different bdnf Val66Met genotypes. 25062900

2015

dbSNP: rs759834365
rs759834365
0.060 GeneticVariation BEFREE Association between BDNF polymorphism (Val66Met) and executive function in patients with amnestic mild cognitive impairment or mild Alzheimer disease. 22699449

2012

dbSNP: rs759834365
rs759834365
0.060 GeneticVariation BEFREE Although Val66Met polymorphisms were not associated with the cross-sectional diagnoses of MCI or AD, the presence of Met-BDNF allele was associated with a higher risk of disease-progression in patients with MCI (OR=3.0 CI(95%) [1.2-7.8], P=0.02). 20491609

2010

dbSNP: rs759834365
rs759834365
0.060 GeneticVariation BEFREE The BDNF Val66Met polymorphism was not associated with serum BDNF or cognitive function in aMCI patients. 18505307

2008

dbSNP: rs11136000
rs11136000
CLU
0.040 GeneticVariation BEFREE Contrary to other studies on Asian populations, this study demonstrated an association between rs11136000 and MCI in an elderly Iranian population. 30560405

2019

dbSNP: rs11136000
rs11136000
CLU
0.040 GeneticVariation BEFREE To evaluate cognitive performance and presence of polymorphisms of the genes SORL1(rs11218304), PVRL2(rs6859), CR1(rs6656401), TOMM40(rs2075650), APOE (isoforms ɛ2, ɛ3, ɛ4), PICALM(rs3851179), GWAS_14q(rs11622883), BIN1(rs744373), and CLU (rs227959 and rs11136000) in patients with MCI and healthy individuals. 30503753

2018

dbSNP: rs11136000
rs11136000
CLU
0.040 GeneticVariation BEFREE CLU-rs11136000-G associated with worse baseline memory and incident MCI/LOAD. 25189118

2015

dbSNP: rs11136000
rs11136000
CLU
0.040 GeneticVariation BEFREE Plasma clusterin levels and the rs11136000 genotype in individuals with mild cognitive impairment and Alzheimer's disease. 24117116

2013

dbSNP: rs4680
rs4680
0.030 GeneticVariation BEFREE These results confirm the importance of the COMTp.Val158Met genotype on tasks assessing attention and cognitive flexibility in midlife but not in healthy aging and the development of MCI. 26489081

2016

dbSNP: rs4680
rs4680
0.030 GeneticVariation BEFREE Influence of COMT Val158Met polymorphism on Alzheimer's disease and mild cognitive impairment in Italian patients. 22890094

2012

dbSNP: rs4680
rs4680
0.030 GeneticVariation BEFREE The COMT Val158 Met polymorphism as an associated risk factor for Alzheimer disease and mild cognitive impairment in APOE 4 carriers. 19793392

2009

dbSNP: rs1416580204
rs1416580204
MOK
0.020 GeneticVariation BEFREE G82S polymorphism of receptor for advanced glycation end products gene and serum soluble RAGE levels in mild cognitive impairment and dementia of Alzheimer's type patients in Turkish population. 30389362

2019

dbSNP: rs2070600
rs2070600
0.020 GeneticVariation BEFREE G82S polymorphism of receptor for advanced glycation end products gene and serum soluble RAGE levels in mild cognitive impairment and dementia of Alzheimer's type patients in Turkish population. 30389362

2019

dbSNP: rs363050
rs363050
0.020 GeneticVariation BEFREE Moreover, distribution of the STX1a rs4717806 allele in SNAP-25 rs363050 AA carriers was significantly different between MCI and HC (p = 0.018). 30958380

2019