Variant: rs886043455 

    present in Gene: LOC107987139;KCNT1
    present in Chromosome: 9
    Position on Chromosome: 135784031
    Alleles of this Variant: G/A;T

rs886043455 in LOC107987139;KCNT1 gene and EPILEPSY, NOCTURNAL FRONTAL LOBE, 5 PMID 26122718 2015 Mutations in KCNT1 cause a spectrum of focal epilepsies.

PMID 27029629 2016 A targeted resequencing gene panel for focal epilepsy.

PMID 29100083 2017 High Rate of Recurrent De Novo Mutations in Developmental and Epileptic Encephalopathies.

rs886043455 in LOC107987139;KCNT1 gene and EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 14 PMID 27029629 2016 A targeted resequencing gene panel for focal epilepsy.

PMID 26122718 2015 Mutations in KCNT1 cause a spectrum of focal epilepsies.

PMID 29100083 2017 High Rate of Recurrent De Novo Mutations in Developmental and Epileptic Encephalopathies.