Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs63750424
rs63750424
0.010 GeneticVariation BEFREE MAPT p.R406W carriers present clinically with progressive memory loss and neuropathologically with neuronal and glial tauopathy. 30546007

2018

dbSNP: rs7695558
rs7695558
0.010 GeneticVariation BEFREE Cognitively normal minor allele carriers of rs7695558 who developed incident AD showed accelerated memory loss prior to disease onset. 29154276

2018

dbSNP: rs6265
rs6265
0.010 GeneticVariation BEFREE While allelic variation in BDNF Val66Met may influence Aβ+ related neurodegeneration and memory loss over the short term, this is not related to serum mBDNF. 28720165

2017

dbSNP: rs759834365
rs759834365
0.010 GeneticVariation BEFREE While allelic variation in BDNF Val66Met may influence Aβ+ related neurodegeneration and memory loss over the short term, this is not related to serum mBDNF. 28720165

2017

dbSNP: rs1217691063
rs1217691063
0.010 GeneticVariation BEFREE In summary, high tHcy per se, or MTHFR C677T TT in combination with the APOE-ε4 allele, might be associated primarily with executive dysfunctions rather than memory loss. 26774227

2016

dbSNP: rs6311
rs6311
0.010 GeneticVariation BEFREE No significant association was found between the SNPs analysed and response to escitalopram in patients with MDD though a significant association was seen between the side effect of memory loss and rs6311. 26261165

2015

dbSNP: rs63749884
rs63749884
0.010 GeneticVariation BEFREE We reported a patient with early-onset FAD and the PSEN2 p.Met239Ile mutation, presenting with severe executive dysfunction and myoclonic tremor, associated with memory loss. 22531416

2012

dbSNP: rs761592007
rs761592007
0.010 GeneticVariation BEFREE We reported a patient with early-onset FAD and the PSEN2 p.Met239Ile mutation, presenting with severe executive dysfunction and myoclonic tremor, associated with memory loss. 22531416

2012

dbSNP: rs28933385
rs28933385
0.010 GeneticVariation BEFREE A missense mutation in codon 200 (E200K) of the PRNP was identified in this patient; CSF 14-3-3 protein was positive; sleep disturbance was the initial sign and the other symptoms gradually appeared, including memory loss, dizziness and ataxia. 20514992

2010

dbSNP: rs767181086
rs767181086
0.010 GeneticVariation BEFREE A missense mutation in codon 200 (E200K) of the PRNP was identified in this patient; CSF 14-3-3 protein was positive; sleep disturbance was the initial sign and the other symptoms gradually appeared, including memory loss, dizziness and ataxia. 20514992

2010