Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs759834365
rs759834365
0.100 GeneticVariation BEFREE BDNF Val66Met polymorphism is associated with cognitive impairment in Italian patients with Parkinson's disease. 19538209

2009

dbSNP: rs6265
rs6265
0.100 GeneticVariation BEFREE This study examines whether BDNF V66M (c.196 G --> A) or NR4A2 IVS6 +18insG polymorphism is associated with the risk of Taiwanese PD and the age of onset using a case-control study. 17427185

2007

dbSNP: rs759834365
rs759834365
0.100 GeneticVariation BEFREE This study examines whether BDNF V66M (c.196 G --> A) or NR4A2 IVS6 +18insG polymorphism is associated with the risk of Taiwanese PD and the age of onset using a case-control study. 17427185

2007

dbSNP: rs6265
rs6265
0.100 GeneticVariation BEFREE To date, there have been several conflicting reports on the correlation between AD or PD and Val66Met or C270T polymorphism in the BDNF promoter region, although no data on this relationship have been published with respect to dementia with Lewy bodies (DLB). 16899999

2006

dbSNP: rs6265
rs6265
0.100 GeneticVariation BEFREE No association between the brain-derived neurotrophic factor 196 G>A or 270 C>T polymorphisms and Alzheimer's or Parkinson's disease. 16565926

2006

dbSNP: rs746682028
rs746682028
0.100 GeneticVariation BEFREE No association between the brain-derived neurotrophic factor 196 G>A or 270 C>T polymorphisms and Alzheimer's or Parkinson's disease. 16565926

2006

dbSNP: rs759834365
rs759834365
0.100 GeneticVariation BEFREE To date, there have been several conflicting reports on the correlation between AD or PD and Val66Met or C270T polymorphism in the BDNF promoter region, although no data on this relationship have been published with respect to dementia with Lewy bodies (DLB). 16899999

2006

dbSNP: rs759834365
rs759834365
0.100 GeneticVariation BEFREE No association between the brain-derived neurotrophic factor 196 G>A or 270 C>T polymorphisms and Alzheimer's or Parkinson's disease. 16565926

2006

dbSNP: rs6265
rs6265
0.100 GeneticVariation BEFREE Overall, the meta-analysis of the allele contrast (A vs G) suggested large heterogeneity between studies (P=0.07, I2 =51%) and no association between G196A and the risk of developing PD: random effects odds ratio (OR)=1.00 [95% CI (0.85, 1.18)]. 16172806

2005

dbSNP: rs746682028
rs746682028
0.100 GeneticVariation BEFREE Overall, the meta-analysis of the allele contrast (A vs G) suggested large heterogeneity between studies (P=0.07, I2 =51%) and no association between G196A and the risk of developing PD: random effects odds ratio (OR)=1.00 [95% CI (0.85, 1.18)]. 16172806

2005

dbSNP: rs759834365
rs759834365
0.100 GeneticVariation BEFREE Overall, the meta-analysis of the allele contrast (A vs G) suggested large heterogeneity between studies (P=0.07, I2 =51%) and no association between G196A and the risk of developing PD: random effects odds ratio (OR)=1.00 [95% CI (0.85, 1.18)]. 16172806

2005

dbSNP: rs6265
rs6265
0.100 GeneticVariation BEFREE We estimated and compared the haplotype frequencies between C270T and G196A markers in PD and controls that was positive (p = 0.0019). 15120095

2004

dbSNP: rs746682028
rs746682028
0.100 GeneticVariation BEFREE We estimated and compared the haplotype frequencies between C270T and G196A markers in PD and controls that was positive (p = 0.0019). 15120095

2004

dbSNP: rs759834365
rs759834365
0.100 GeneticVariation BEFREE We estimated and compared the haplotype frequencies between C270T and G196A markers in PD and controls that was positive (p = 0.0019). 15120095

2004

dbSNP: rs6265
rs6265
0.100 GeneticVariation BEFREE Thus, our negative findings suggest that it is unlikely that the BDNF Val66Met polymorphism plays a major role in the pathogenesis of PD in the Chinese population. 14642442

2003

dbSNP: rs759834365
rs759834365
0.100 GeneticVariation BEFREE Thus, our negative findings suggest that it is unlikely that the BDNF Val66Met polymorphism plays a major role in the pathogenesis of PD in the Chinese population. 14642442

2003

dbSNP: rs6265
rs6265
0.100 GeneticVariation BEFREE We found that homozygosity for the V66M polymorphism of the brain-derived neurotrophic factor (BDNF) gene occurs more frequently in patients with Parkinson's disease than in unaffected controls (chi(2) = 5.46) and confirmed an association with the S18Y polymorphism of the UCH-L1 gene. 11782995

2002

dbSNP: rs759834365
rs759834365
0.100 GeneticVariation BEFREE We found that homozygosity for the V66M polymorphism of the brain-derived neurotrophic factor (BDNF) gene occurs more frequently in patients with Parkinson's disease than in unaffected controls (chi(2) = 5.46) and confirmed an association with the S18Y polymorphism of the UCH-L1 gene. 11782995

2002

dbSNP: rs764254110
rs764254110
0.030 GeneticVariation BEFREE Gami-Chunggan Formula Prevents Motor Dysfunction in MPTP/p-Induced and A53T α-Synuclein Overexpressed Parkinson's Disease Mouse Model Though DJ-1 and BDNF Expression. 31555122

2019

dbSNP: rs764254110
rs764254110
0.030 GeneticVariation BEFREE FTY720 (fingolimod) reduces synucleinopathy in A53T aSyn mice and motor dysfunction in 6-OHDA and rotenone PD models, but no one has tested FTY720 in mice that develop age-onset PD-like motor problems. 31129200

2019

dbSNP: rs764254110
rs764254110
0.030 GeneticVariation BEFREE We previously found that aging A53T transgenic (Tg) mice closely model PD-like ENS aSyn pathology, making them appropriate for testing potential PD therapies. 27528608

2016

dbSNP: rs893924483
rs893924483
0.010 GeneticVariation BEFREE To determine whether dopaminergic (rs1076560 DRD2 G > T and rs4680 catechole-o-methyltranspherase (COMT) Val158Met) or brain derived neurotrophic factor (rs6265 BDNF Val66Met) genetic polymorphisms are associated with gait function and medication responsiveness in Parkinson's disease. 29249680

2018

dbSNP: rs370102323
rs370102323
0.010 GeneticVariation BEFREE We studied two genetic polymorphisms (240C/T and 480G/A) of the brain-derived neurotrophic factor (BDNF) gene in Japanese patients with Alzheimer's disease (AD, n = 172), Parkinson's disease (PD, n = 327), and multiple system atrophy (MSA, n = 122), as well as controls (n = 275). 15838855

2005