rs3773364, SYN2

N. diseases: 2
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
0.030 GeneticVariation BEFREE No significant association was found between rs2920502 and rs3773364-rs3755724-rs2920502 haplotypes for susceptibility to epilepsy in each ethnicity. 25595263 2015
Epilepsy
CUI: C0014544
Disease: Epilepsy
0.030 GeneticVariation BEFREE Our study indicated that SYN2 rs3773364 A>G polymorphism is not a risk factor for susceptibility to epilepsy. 21465568 2011
Epilepsy
CUI: C0014544
Disease: Epilepsy
0.030 GeneticVariation BEFREE We selected rs3773364 A>G polymorphism in SYN2 gene and analyzed its distribution in north Indian patients with epilepsy and control subjects. 20034013 2010