Variant: rs1564351388 

    present in Gene: STXBP1
    present in Chromosome: 9
    Position on Chromosome: 127666193
    Alleles of this Variant: -/T

rs1564351388 in STXBP1 gene and Abnormal coordination PMID 26865513 2016 STXBP1 encephalopathy: A neurodevelopmental disorder including epilepsy.

rs1564351388 in STXBP1 gene and Epileptic Encephalopathy, Early Infantile, 4 PMID 26865513 2016 STXBP1 encephalopathy: A neurodevelopmental disorder including epilepsy.

rs1564351388 in STXBP1 gene and Global developmental delay PMID 26865513 2016 STXBP1 encephalopathy: A neurodevelopmental disorder including epilepsy.

rs1564351388 in STXBP1 gene and Infantile Spasm PMID 26865513 2016 STXBP1 encephalopathy: A neurodevelopmental disorder including epilepsy.