Variant: rs1057516076 

    present in Gene: KCNQ2-AS1;KCNQ2
    present in Chromosome: 20
    Position on Chromosome: 63446794
    Alleles of this Variant: T/C

rs1057516076 in KCNQ2-AS1;KCNQ2 gene and SEIZURES, BENIGN FAMILIAL NEONATAL, 1 PMID 25982755 2015 Familial neonatal seizures in 36 families: Clinical and genetic features correlate with outcome.

PMID 20298421 2010 EFNS guidelines on the molecular diagnosis of channelopathies, epilepsies, migraine, stroke, and dementias.