rs2304016, SCN2A

N. diseases: 2
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Epilepsy, Generalized
CUI: C0014548
Disease: Epilepsy, Generalized
0.010 GeneticVariation BEFREE SCN2A rs2304016 (<i>P</i> = 0.04) and GRM4 rs2499697 (<i>P</i> = 0.031) were statistically significant with generalized epilepsy. 31297029 2019
Epilepsy
CUI: C0014544
Disease: Epilepsy
0.010 GeneticVariation BEFREE This study identified no significant associations of allelic or genotypic SNPs with the susceptibility of epilepsy and medication response with an exception of rs2304016 and rs2499697 SNPs that were associated with the generalized type of epilepsy among Jordanian population. 31297029 2019