Variant: rs886040861 

    present in Gene: GRIN2D
    present in Chromosome: 19
    Position on Chromosome: 48419722
    Alleles of this Variant: G/A

rs886040861 in GRIN2D gene and EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 46 PMID 27616483 2016 GRIN2D Recurrent De Novo Dominant Mutation Causes a Severe Epileptic Encephalopathy Treatable with NMDA Receptor Channel Blockers.