Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
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: rs1977412
rs1977412
C 0.700 GeneticVariation GWASCAT Genetic data and cognitively defined late-onset Alzheimer's disease subgroups. 30514930

2018

dbSNP: rs2732260
rs2732260
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: 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 Mitochondrial disorder associated with newborn cardiopulmonary arrest. 8511015

1993

dbSNP: rs104894396
rs104894396
T 0.700 CausalMutation CLINVAR

dbSNP: rs1163944538
rs1163944538
GA 0.700 CausalMutation CLINVAR

dbSNP: rs1352010373
rs1352010373
C 0.700 CausalMutation CLINVAR

dbSNP: rs148881970
rs148881970
G 0.700 CausalMutation CLINVAR

dbSNP: rs1554317002
rs1554317002
T 0.700 GeneticVariation CLINVAR

dbSNP: rs1555735545
rs1555735545
A 0.700 CausalMutation CLINVAR

dbSNP: rs28937900
rs28937900
A 0.700 CausalMutation CLINVAR

dbSNP: rs370717845
rs370717845
A 0.700 CausalMutation CLINVAR

dbSNP: rs555145190
rs555145190
T 0.700 CausalMutation CLINVAR

dbSNP: rs63751011
rs63751011
T 0.700 CausalMutation CLINVAR

dbSNP: rs768823392
rs768823392
A 0.700 CausalMutation CLINVAR

dbSNP: rs80356702
rs80356702
A 0.700 GeneticVariation CLINVAR

dbSNP: rs63751273
rs63751273
0.030 GeneticVariation BEFREE Expression of P301L-hTau in mouse MEC induces hippocampus-dependent memory deficit. 28634382

2017

dbSNP: rs63751273
rs63751273
0.030 GeneticVariation BEFREE The present study was undertaken to examine whether lycopene or lycopene/vitamin E could exert protective effects on memory deficit and oxidative stress in tau transgenic mice expressing P301L mutation. 28269786

2017

dbSNP: rs6265
rs6265
0.030 GeneticVariation BEFREE BDNF Val66Met moderates memory impairment, hippocampal function and tau in preclinical autosomal dominant Alzheimer's disease. 27521573

2016

dbSNP: rs759834365
rs759834365
0.030 GeneticVariation BEFREE BDNF Val66Met moderates memory impairment, hippocampal function and tau in preclinical autosomal dominant Alzheimer's disease. 27521573

2016

dbSNP: rs6265
rs6265
0.030 GeneticVariation BEFREE A Val(66)Met single-nucleotide polymorphism (SNP) in the brain-derived neurotrophic factor (BDNF) gene impairs activity-dependent BDNF release in cultured hippocampal neurons and predicts impaired memory and exaggerated basal hippocampal activity in healthy humans. 23319002

2013

dbSNP: rs759834365
rs759834365
0.030 GeneticVariation BEFREE A Val(66)Met single-nucleotide polymorphism (SNP) in the brain-derived neurotrophic factor (BDNF) gene impairs activity-dependent BDNF release in cultured hippocampal neurons and predicts impaired memory and exaggerated basal hippocampal activity in healthy humans. 23319002

2013

dbSNP: rs63751273
rs63751273
0.030 GeneticVariation BEFREE Forebrain-specific over-expression of human tau(P301L), a mutation associated with frontotemporal dementia with parkinsonism linked to chromosome 17, in rTg4510 mice results in the formation of NFTs, learning and memory impairment and massive neuronal death. 22027994

2012