Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs6265
rs6265
BDNF ; BDNF-AS
0.020 GeneticVariation BEFREE We did not find any evidence supporting the association of the BDNF Val66Met polymorphism with primary dystonia. 24925604

2014
dbSNP: rs759834365
rs759834365
BDNF ; BDNF-AS
0.020 GeneticVariation BEFREE We did not find any evidence supporting the association of the BDNF Val66Met polymorphism with primary dystonia. 24925604

2014
dbSNP: rs1801968
rs1801968
TOR1A
0.020 GeneticVariation BEFREE The purpose of this study is to evaluate the D216H polymorphism in an Argentinean cohort of 40 patients with primary dystonia and 200 unrelated control subjects. 23405979

2013
dbSNP: rs6265
rs6265
BDNF ; BDNF-AS
0.020 GeneticVariation BEFREE Our findings do not support that BDNF Val66Met polymorphism contributes to the risk of primary dystonia. 23201631

2013
dbSNP: rs759834365
rs759834365
BDNF ; BDNF-AS
0.020 GeneticVariation BEFREE Our findings do not support that BDNF Val66Met polymorphism contributes to the risk of primary dystonia. 23201631

2013
dbSNP: rs1801968
rs1801968
TOR1A
0.020 GeneticVariation BEFREE Our findings do not confirm that the allele contributes to the risk of D216H SNP primary dystonia. 22054283

2012
dbSNP: rs587776983
rs587776983
TUBB4A
0.010 GeneticVariation BEFREE The c.4C>G DYT4 mutation appears to be private, and clinical testing for TUBB4A mutations is not justified in spasmodic dysphonia or other forms of primary dystonia. 24598712

2014
dbSNP: rs1182
rs1182
TOR1A
0.010 GeneticVariation BEFREE Association of rs1182 polymorphism of the DYT1 gene with primary dystonia in Chinese population. 23058565

2012