Variant: rs796053124 

    present in Gene: SCN2A
    present in Chromosome: 2
    Position on Chromosome: 165354232
    Alleles of this Variant: G/T

rs796053124 in SCN2A gene and Epilepsy PMID 20956790 2010 SCN2A mutation associated with neonatal epilepsy, late-onset episodic ataxia, myoclonus, and pain.

rs796053124 in SCN2A gene and Episodic Ataxia PMID 20956790 2010 SCN2A mutation associated with neonatal epilepsy, late-onset episodic ataxia, myoclonus, and pain.

rs796053124 in SCN2A gene and Vertigo PMID 20956790 2010 SCN2A mutation associated with neonatal epilepsy, late-onset episodic ataxia, myoclonus, and pain.