Variant: rs35450031 

    present in Gene: KCNQ2;LOC105372724
    present in Chromosome: 20
    Position on Chromosome: 63413524
    Alleles of this Variant: G/A;C

rs35450031 in KCNQ2;LOC105372724 gene and EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 7 PMID 23621294 2013 Clinical spectrum of early onset epileptic encephalopathies caused by KCNQ2 mutation.