Variant: rs137852681 

    present in Gene: CLCN2
    present in Chromosome: 3
    Position on Chromosome: 184352810
    Alleles of this Variant: C/T

rs137852681 in CLCN2 gene and EPILEPSY, IDIOPATHIC GENERALIZED, SUSCEPTIBILITY TO, 11 PMID 19710712 2009 CLCN2 variants in idiopathic generalized epilepsy.