Variant: rs1057516077 

    present in Gene: KCNQ2-AS1;KCNQ2
    present in Chromosome: 20
    Position on Chromosome: 63446793
    Alleles of this Variant: G/A

rs1057516077 in KCNQ2-AS1;KCNQ2 gene and EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 7 PMID 22926866 2012 Whole exome sequencing identifies KCNQ2 mutations in Ohtahara syndrome.