Variant: rs118192197 

    present in Gene: KCNQ2
    present in Chromosome: 20
    Position on Chromosome: 63444756
    Alleles of this Variant: CGGAGCGCAG/T

rs118192197 in KCNQ2 gene and EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 1 PMID 16235065 2005 Functional analysis of novel KCNQ2 and KCNQ3 gene variants found in a large pedigree with benign familial neonatal convulsions (BFNC).