Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs602594
rs602594
Entrez Id: 6327
Gene Symbol: SCN2B
SCN2B
CUI: C0391957
Disease:
idiopathic epilepsy
0.010 GeneticVariation BEFREE SCN1A rs2298771 was associated in Indians (OR = 0.56, p = 0.005) and SCN2B rs602594 with idiopathic epilepsy (OR = 0.62, p = 0.002). 24337656 2014