Variant: rs1057516084 

    present in Gene: KCNQ2
    present in Chromosome: 20
    Position on Chromosome: 63444755
    Alleles of this Variant: CCG/T

rs1057516084 in KCNQ2 gene and SEIZURES, BENIGN FAMILIAL NEONATAL, 1 PMID 23360469 2013 Genetic testing in benign familial epilepsies of the first year of life: clinical and diagnostic significance.