Variant: rs755440336 

    present in Gene: SCN3A
    present in Chromosome: 2
    Position on Chromosome: 165131366
    Alleles of this Variant: C/T

rs755440336 in SCN3A gene and EPILEPSY, FAMILIAL FOCAL, WITH VARIABLE FOCI 4 PMID 28235671 2017 SCN3A deficiency associated with increased seizure susceptibility.

PMID 24157691 2014 Novel SCN3A variants associated with focal epilepsy in children.