Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
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: 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