Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs121908225
rs121908225
CACNA1A
0.040 GeneticVariation BEFREE Genetic analysis of familial hemiplegic migraine revealed a heterozygous S218L mutation in CACNA1A. 21824570

2011
dbSNP: rs121908225
rs121908225
CACNA1A
0.040 GeneticVariation BEFREE The CACNA1A S218L mutation is associated with familial hemiplegic migraine, ataxia and/or ESCEATHT. 19520699

2009
dbSNP: rs121908225
rs121908225
CACNA1A
0.040 GeneticVariation BEFREE The S218L familial hemiplegic migraine mutation promotes deinhibition of Ca(v)2.1 calcium channels during direct G-protein regulation. 18581134

2008
dbSNP: rs121908225
rs121908225
CACNA1A
0.040 GeneticVariation BEFREE Electroencephalographic changes and seizures in familial hemiplegic migraine patients with the CACNA1A gene S218L mutation. 18313928

2008