Variant: rs118192212 

    present in Gene: KCNQ2
    present in Chromosome: 20
    Position on Chromosome: 63439610
    Alleles of this Variant: AAG/-

rs118192212 in KCNQ2 gene and Benign Rolandic Epilepsy PMID 18640800 2009 A de novo KCNQ2 mutation detected in non-familial benign neonatal convulsions.

PMID 22884718 2012 KCNQ2 abnormality in BECTS: benign childhood epilepsy with centrotemporal spikes following benign neonatal seizures resulting from a mutation of KCNQ2.