Variant: rs118192192 

    present in Gene: KCNQ2-AS1;KCNQ2
    present in Chromosome: 20
    Position on Chromosome: 63446786
    Alleles of this Variant: CTT/-

rs118192192 in KCNQ2-AS1;KCNQ2 gene and EPILEPSY, BENIGN NEONATAL, 2 PMID 19464834 2009 Sodium and potassium channel dysfunctions in rare and common idiopathic epilepsy syndromes.

PMID 18625963 2008 KCNQ2 and KCNQ3 mutations contribute to different idiopathic epilepsy syndromes.