Variant: rs138450474 

    present in Gene: HPN;SCN1B
    present in Chromosome: 19
    Position on Chromosome: 35039140
    Alleles of this Variant: G/A;C

rs138450474 in HPN;SCN1B gene and Epilepsy, Rolandic PMID 29358611 2018 Exome-wide analysis of mutational burden in patients with typical and atypical Rolandic epilepsy.