Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs104893877
rs104893877
SNCA
0.020 GeneticVariation BEFREE A53T mice also exhibit spatial memory deficits at 6 and 12 months, as demonstrated by Y-maze performance. 23936403

2013
dbSNP: rs104893877
rs104893877
SNCA
0.020 GeneticVariation BEFREE Our results directly implicate tau as a mediator of specific human mutant A53T αS-mediated abnormalities related to deficits in hippocampal neurotransmission and suggest a mechanism for memory impairment that occurs as a consequence of synaptic dysfunction rather than synaptic or neuronal loss. 31168644

2019
dbSNP: rs104894396
rs104894396
GJB2
T 0.700 CausalMutation CLINVAR

dbSNP: rs11136000
rs11136000
CLU
0.010 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: rs11142387
rs11142387 		0.010 GeneticVariation BEFREE In particular, carrying the A allele of rs11142387 near KLF9 was found to be associated with psychiatric disease and poor memory performance, which warrants further investigations. 27923415

2017
dbSNP: rs1163944538
rs1163944538
TMEM94
GA 0.700 CausalMutation CLINVAR

dbSNP: rs12273363
rs12273363
BDNF
0.010 GeneticVariation BEFREE Specifically, we examined nine BDNF single-nucleotide polymorphisms (SNPs; rs908867, rs11030094, rs6265, rs10501087, rs1157659, rs1491850, rs11030107, rs7127507 and rs12273363) previously associated with brain atrophy or memory deficits in mTBI. 28755387

2018
dbSNP: rs1352010373
rs1352010373
TMEM94
C 0.700 CausalMutation CLINVAR

dbSNP: rs1397094538
rs1397094538
ZNF436 ; ZNF436-AS1
0.010 GeneticVariation BEFREE We found a causal role for T158A mutation in the development of RTT-like phenotypes, including developmental regression, motor dysfunction, and learning and memory deficits. 22119903

2011
dbSNP: rs1411832
rs1411832
LOC105378469
0.010 GeneticVariation BEFREE On associating quantitative DMS-TC with interactive variables of groups × genotype, one SNP (rs1411832), located downstream of YWHAZP5 in chromosome 10, was found to be associated with the working memory deficit in schizophrenia patients with lowest p-value (p = 2.02 × 10(-7)). 25608650

2015
dbSNP: rs1424266770
rs1424266770
CASP3
0.010 GeneticVariation BEFREE H63D mutation in hemochromatosis alters cholesterol metabolism and induces memory impairment. 24439478

2014
dbSNP: rs148881970
rs148881970
NAGLU
G 0.700 CausalMutation CLINVAR

dbSNP: rs1554317002
rs1554317002
CDK13 ; LOC112267983
T 0.700 GeneticVariation CLINVAR

dbSNP: rs1555735545
rs1555735545
STRN4 ; FKRP
A 0.700 CausalMutation CLINVAR

dbSNP: rs1556424691
rs1556424691
CYTB ; ND6 ; TRNT
G 0.700 CausalMutation CLINVAR Mitochondrial disorder associated with newborn cardiopulmonary arrest. 8511015

1993
dbSNP: rs1556424691
rs1556424691
CYTB ; ND6 ; TRNT
G 0.700 CausalMutation CLINVAR New mitochondrial DNA mutations in tRNA associated with three severe encephalopamyopathic phenotypes: neonatal, infantile, and childhood onset. 22638997

2012
dbSNP: rs1556424691
rs1556424691
CYTB ; ND6 ; TRNT
G 0.700 CausalMutation CLINVAR Mutation m.15923A>G in the MT-TT gene causes mild myopathy - case report of an adult-onset phenotype. 30236074

2018
dbSNP: rs1556424691
rs1556424691
CYTB ; ND6 ; TRNT
G 0.700 CausalMutation CLINVAR CO2-sensitive tRNA modification associated with human mitochondrial disease. 29760464

2018
dbSNP: rs17125721
rs17125721
PSEN1
0.010 GeneticVariation BEFREE Association between the presenilin-1 mutation Glu318Gly and complaints of memory impairment. 11755019

2002
dbSNP: rs1799945
rs1799945
HFE ; LOC108783645
0.010 GeneticVariation BEFREE H63D mutation in hemochromatosis alters cholesterol metabolism and induces memory impairment. 24439478

2014
dbSNP: rs1977412
rs1977412
LOC105373166
C 0.700 GeneticVariation GWASCAT Genetic data and cognitively defined late-onset Alzheimer's disease subgroups. 30514930

2018
dbSNP: rs2732260
rs2732260
FUT10
A 0.700 GeneticVariation GWASCAT Potential genetic modifiers of disease risk and age at onset in patients with frontotemporal lobar degeneration and GRN mutations: a genome-wide association study. 29724592

2018
dbSNP: rs281865071
rs281865071
CHRNB2
0.020 GeneticVariation BEFREE Autosomal dominant nocturnal frontal lobe epilepsy and mild memory impairment associated with CHRNB2 mutation I312M in the neuronal nicotinic acetylcholine receptor. 18534914

2008
dbSNP: rs281865071
rs281865071
CHRNB2
0.020 GeneticVariation BEFREE The CHRNB2 mutation I312M is associated with epilepsy and distinct memory deficits. 15964197

2005
dbSNP: rs28937900
rs28937900
FKRP
A 0.700 CausalMutation CLINVAR