Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs28933400
rs28933400
ATP1A2
0.020 GeneticVariation BEFREE Twelve familial hemiplegic migraine (FHM) patients (6 with the I1811L mutation in CACNA1A, 3 with M731T mutation in ATP1A2, and 3 without known mutations) and 10 control subjects underwent single-fiber EMG. 15557518

2004
dbSNP: rs28933400
rs28933400
ATP1A2
0.020 GeneticVariation BEFREE The M731T mutation was found in a family with pure FHM. 12953268

2003