Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs2230288
rs2230288
GBA
0.020 GeneticVariation BEFREE Also, we replicated previous reports of GBA coding variants (rs2230288: p.E365K; rs75548401: p.T408M) being associated with greater motor and cognitive decline over time, and an APOE E4 tagging variant (rs429358) being associated with greater cognitive deficits in patients. 31505070

2019

dbSNP: rs2230288
rs2230288
GBA
0.020 GeneticVariation BEFREE Also, we replicated previous reports of GBA coding variants (rs2230288: p.E365K; rs75548401: p.T408M) being associated with greater motor and cognitive decline over time, and an APOE E4 tagging variant (rs429358) being associated with greater cognitive deficits in patients. 31505070

2019

dbSNP: rs6265
rs6265
0.020 GeneticVariation BEFREE <i>BDNF</i> gene Val66Met variation may be associated with cognitive deficits in T2DM, especially with delayed memory. 29423073

2018

dbSNP: rs759834365
rs759834365
0.020 GeneticVariation BEFREE <i>BDNF</i> gene Val66Met variation may be associated with cognitive deficits in T2DM, especially with delayed memory. 29423073

2018

dbSNP: rs34637584
rs34637584
0.020 GeneticVariation BEFREE The objective of this study was to determine whether human LRRK2 with G2019S mutation causes hippocampus-dependent cognitive deficits in mice. 28487191

2017

dbSNP: rs2230288
rs2230288
GBA
0.020 GeneticVariation BEFREE The discovery that E326K negatively impacts cognitive performance approximately doubles the proportion of PD patients we now recognize are at risk for more severe GBA-related cognitive deficits. 26296077

2016

dbSNP: rs34637584
rs34637584
0.020 GeneticVariation BEFREE Contrastingly, high levels of human LRRK2 cause locomotor alterations and cognitive deficits accompanied by reduced striatal dopamine levels, with the latter also observed in G2019S mutant mice. 26282470

2015

dbSNP: rs6265
rs6265
0.020 GeneticVariation BEFREE The BDNF Val66Met polymorphism, resting-state hippocampal functional connectivity and cognitive deficits in acute late-onset depression. 26000753

2015

dbSNP: rs759834365
rs759834365
0.020 GeneticVariation BEFREE The BDNF Val66Met polymorphism, resting-state hippocampal functional connectivity and cognitive deficits in acute late-onset depression. 26000753

2015

dbSNP: rs371425292
rs371425292
APP
0.020 GeneticVariation BEFREE In this study, we examined the effect of obovatol on cognitive deficits in two separate AD models: (i) mice that received intracerebroventricular (i.c.v.) infusion of Aβ(1-42) (2.0 μg/mouse) and (ii) Tg2576 mice-expressing mutant human amyloid precursor protein (K670N, M671L). 22212065

2012

dbSNP: rs572842823
rs572842823
APP
0.020 GeneticVariation BEFREE In this study, we examined the effect of obovatol on cognitive deficits in two separate AD models: (i) mice that received intracerebroventricular (i.c.v.) infusion of Aβ(1-42) (2.0 μg/mouse) and (ii) Tg2576 mice-expressing mutant human amyloid precursor protein (K670N, M671L). 22212065

2012

dbSNP: rs371425292
rs371425292
APP
0.020 GeneticVariation BEFREE Both synaptic and cognitive deficits are reproduced in mice double transgenic for amyloid precursor protein (AA substitution K670N,M671L) and presenilin-1 (AA substitution M146V). 15578094

2004

dbSNP: rs572842823
rs572842823
APP
0.020 GeneticVariation BEFREE Both synaptic and cognitive deficits are reproduced in mice double transgenic for amyloid precursor protein (AA substitution K670N,M671L) and presenilin-1 (AA substitution M146V). 15578094

2004

dbSNP: rs10748842
rs10748842
0.010 GeneticVariation BEFREE NRG3 rs10748842 may not confer susceptibility to schizophrenia, but may be more closely associated with cognitive deficit, especially attention performance in chronic schizophrenia. 31753594

2020

dbSNP: rs104893878
rs104893878
0.010 GeneticVariation BEFREE TCE or TaClo did not appear to lead to acceleration of motor or cognitive deficits in either wild type or A30P mutant mice, potentially because of the modest reductions of DA neuronal number in the SNpc. 31422098

2019

dbSNP: rs11136000
rs11136000
CLU
0.010 GeneticVariation BEFREE The rs11136000 genotypes in combination with HDL levels and knowledge about diabetes background may be used as a predictive medicine tool for cognitive disorders. 30560405

2019

dbSNP: rs16969968
rs16969968
0.010 GeneticVariation BEFREE Our results show that rs16969968 on CHRNA5 is tightly linked to genetic susceptibility, psychotic symptoms and cognitive deficits in SCZ in an early-onset Chinese population, suggesting that CHRNA5 may play an important role in the etiology of SCZ. 30366711

2019

dbSNP: rs429358
rs429358
0.010 GeneticVariation BEFREE Also, we replicated previous reports of GBA coding variants (rs2230288: p.E365K; rs75548401: p.T408M) being associated with greater motor and cognitive decline over time, and an APOE E4 tagging variant (rs429358) being associated with greater cognitive deficits in patients. 31505070

2019

dbSNP: rs75548401
rs75548401
GBA
0.010 GeneticVariation BEFREE Also, we replicated previous reports of GBA coding variants (rs2230288: p.E365K; rs75548401: p.T408M) being associated with greater motor and cognitive decline over time, and an APOE E4 tagging variant (rs429358) being associated with greater cognitive deficits in patients. 31505070

2019

dbSNP: rs761715536
rs761715536
0.010 GeneticVariation BEFREE Also, we replicated previous reports of GBA coding variants (rs2230288: p.E365K; rs75548401: p.T408M) being associated with greater motor and cognitive decline over time, and an APOE E4 tagging variant (rs429358) being associated with greater cognitive deficits in patients. 31505070

2019

dbSNP: rs104893877
rs104893877
0.010 GeneticVariation BEFREE Here we first provided evidence that RV treatment alleviated motor and cognitive deficits in the A53T α-synuclein mouse model of PD in a dose-dependent manner. 30462117

2018

dbSNP: rs1108580
rs1108580
DBH
0.010 GeneticVariation BEFREE This study examines the association of plasma DβH (pDβH) activity, DBH gene polymorphisms (-1021C>T, rs1611115 and 444G>A, rs1108580) and cognitive deficits in Han Chinese patients with schizophrenia. 28647493

2018

dbSNP: rs121909668
rs121909668
FUS
0.010 GeneticVariation BEFREE Sleep and circadian abnormalities precede cognitive deficits in R521C FUS knockin rats. 30273830

2018

dbSNP: rs1611115
rs1611115
DBH
0.010 GeneticVariation BEFREE This study examines the association of plasma DβH (pDβH) activity, DBH gene polymorphisms (-1021C>T, rs1611115 and 444G>A, rs1108580) and cognitive deficits in Han Chinese patients with schizophrenia. 28647493

2018

dbSNP: rs63751273
rs63751273
0.010 GeneticVariation BEFREE Here, we studied the effects of P301L hTau transduction in the medial EC (MEC) of mice on tau phosphorylation and accumulation, and cognitive deficit. 28634382

2017