Variant: rs1057516106 

    present in Gene: LOC105372721;KCNQ2
    present in Chromosome: 20
    Position on Chromosome: 63433876
    Alleles of this Variant: G/A;C

rs1057516106 in LOC105372721;KCNQ2 gene and SEIZURES, BENIGN FAMILIAL NEONATAL, 1 PMID 24375629 2014 Novel KCNQ2 and KCNQ3 mutations in a large cohort of families with benign neonatal epilepsy: first evidence for an altered channel regulation by syntaxin-1A.