rs759834365, BDNF-AS;BDNF

N. diseases: 237
Disease: Epilepsy ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Epilepsy
CUI: C0014544
Disease: Epilepsy
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
Epilepsy
CUI: C0014544
Disease: Epilepsy
0.050 GeneticVariation BEFREE However, whether BDNF Val66Met polymorphism is associated with epilepsy remains controversial. 26000807 2016
Epilepsy
CUI: C0014544
Disease: Epilepsy
0.050 GeneticVariation BEFREE Predisposition to epilepsy in fragile X syndrome: does the Val66Met polymorphism in the BDNF gene play a role? 21890420 2011
Epilepsy
CUI: C0014544
Disease: Epilepsy
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
Epilepsy
CUI: C0014544
Disease: Epilepsy
0.050 GeneticVariation BEFREE The Val66Met polymorphism in the BDNF gene is associated with epilepsy in fragile X syndrome. 19394799 2009