Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs121908225
rs121908225
CACNA1A
0.020 GeneticVariation BEFREE Here we report a sporadic case of FHM1 linked to S218L CACNA1A gene mutation with the triad of prolonged hemiplegic migraine, cerebellar symptoms, and epileptic seizures. 20071244

2010
dbSNP: rs121908225
rs121908225
CACNA1A
0.020 GeneticVariation BEFREE The case history we report suggests a specific, severe phenotype and the co-occurrence of HM and epilepsy related to the S218L FHM1 mutation. 19438926

2009