Variant: rs1553245771 

    present in Gene: ATP1A2
    present in Chromosome: 1
    Position on Chromosome: 160135461
    Alleles of this Variant: G/A

rs1553245771 in ATP1A2 gene and Familial Hemiplegic Migraine PMID 21352219 2011 Prolonged sporadic hemiplegic migraine associated with a novel de novo missense ATP1A2 gene mutation.

rs1553245771 in ATP1A2 gene and MIGRAINE, FAMILIAL HEMIPLEGIC, 2 PMID 23918834 2014 A novel ATP1A2 gene mutation in familial hemiplegic migraine and epilepsy.

PMID 23838748 2013 Functional characterization of a novel C-terminal ATP1A2 mutation causing hemiplegic migraine and epilepsy.

PMID 12953268 2003 Novel mutations in the Na+, K+-ATPase pump gene ATP1A2 associated with familial hemiplegic migraine and benign familial infantile convulsions.

PMID 12539047 2003 Haploinsufficiency of ATP1A2 encoding the Na+/K+ pump alpha2 subunit associated with familial hemiplegic migraine type 2.

PMID 21352219 2011 Prolonged sporadic hemiplegic migraine associated with a novel de novo missense ATP1A2 gene mutation.