Disease: Hemiplegic migraine, familial type 1 ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs28933401
rs28933401
Entrez Id: 477
Gene Symbol: ATP1A2
ATP1A2
CUI: C1832884
Disease:
Hemiplegic migraine, familial type 1 		0.010 GeneticVariation BEFREE The R689Q mutation was identified in a family in which FHM and benign familial infantile convulsions partially cosegregate. 12953268 2003