Disease: MIGRAINE, SPORADIC HEMIPLEGIC ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1553245771
rs1553245771
Entrez Id: 477
Gene Symbol: ATP1A2
ATP1A2
CUI: C1832903
Disease:
MIGRAINE, SPORADIC HEMIPLEGIC 		0.010 GeneticVariation BEFREE There are familial and sporadic cases, both on a genetic basis; we describe the case of a 6-year-old boy affected by sporadic hemiplegic migraine, showing a novel ATP1A2 gene missense mutation (p.Gly715Arg) in exon 16. 21352219 2011