Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs759834365
rs759834365
BDNF ; BDNF-AS
0.050 GeneticVariation BEFREE Mann-Whitney U, t-tests, and Fisher's exact tests were used to determine if APOE4, BDNF Val66Met, or COMT Val158Met are associated with increased psychiatric symptomatology in people with epilepsy. 30909076

2019
dbSNP: rs759834365
rs759834365
BDNF ; BDNF-AS
0.050 GeneticVariation BEFREE However, whether BDNF Val66Met polymorphism is associated with epilepsy remains controversial. 26000807

2016
dbSNP: rs759834365
rs759834365
BDNF ; BDNF-AS
0.050 GeneticVariation BEFREE Predisposition to epilepsy in fragile X syndrome: does the Val66Met polymorphism in the BDNF gene play a role? 21890420

2011
dbSNP: rs759834365
rs759834365
BDNF ; BDNF-AS
0.050 GeneticVariation BEFREE Moreover, the Val66Met polymorphisms did not influence age of epilepsy onset, duration of epilepsy, control of seizures, or extension of the irritative zone. 19896331

2010
dbSNP: rs759834365
rs759834365
BDNF ; BDNF-AS
0.050 GeneticVariation BEFREE The Val66Met polymorphism in the BDNF gene is associated with epilepsy in fragile X syndrome. 19394799

2009