Variant: rs118192213 

    present in Gene: KCNQ2
    present in Chromosome: 20
    Position on Chromosome: 63438708
    Alleles of this Variant: -/C

rs118192213 in KCNQ2 gene and EPILEPSY, BENIGN NEONATAL, 2 PMID 17129708 2007 Benign familial neonatal convulsions: always benign?