Variant: rs1057516032 

    present in Gene: ATP1A3
    present in Chromosome: 19
    Position on Chromosome: 41970211
    Alleles of this Variant: AGTCT/GA

rs1057516032 in ATP1A3 gene and ALTERNATING HEMIPLEGIA OF CHILDHOOD 2 PMID 26938784 2016 A prospective evaluation of whole-exome sequencing as a first-tier molecular test in infants with suspected monogenic disorders.

rs1057516032 in ATP1A3 gene and Generalized hypotonia PMID 26938784 2016 A prospective evaluation of whole-exome sequencing as a first-tier molecular test in infants with suspected monogenic disorders.

rs1057516032 in ATP1A3 gene and Seizures PMID 26938784 2016 A prospective evaluation of whole-exome sequencing as a first-tier molecular test in infants with suspected monogenic disorders.

rs1057516032 in ATP1A3 gene and Stroke-like episode PMID 26938784 2016 A prospective evaluation of whole-exome sequencing as a first-tier molecular test in infants with suspected monogenic disorders.