Variant: rs1553798675 

    present in Gene: FGF12
    present in Chromosome: 3
    Position on Chromosome: 192335441
    Alleles of this Variant: C/T

rs1553798675 in FGF12 gene and Delayed speech and language development PMID 27872899 2016 De novo FGF12 mutation in 2 patients with neonatal-onset epilepsy.

rs1553798675 in FGF12 gene and EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 47 PMID 27872899 2016 De novo FGF12 mutation in 2 patients with neonatal-onset epilepsy.

rs1553798675 in FGF12 gene and Seizures PMID 27872899 2016 De novo FGF12 mutation in 2 patients with neonatal-onset epilepsy.

rs1553798675 in FGF12 gene and Tonic - clonic seizures PMID 27872899 2016 De novo FGF12 mutation in 2 patients with neonatal-onset epilepsy.