Variant: rs1057516105 

    present in Gene: KCNQ2;LOC105372721
    present in Chromosome: 20
    Position on Chromosome: 63433897
    Alleles of this Variant: A/G

rs1057516105 in KCNQ2;LOC105372721 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.