Source: ALL

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs121908212
rs121908212
CACNA1A
CUI: C0338480
Disease: Common Migraine
Common Migraine 		0.010 GeneticVariation BEFREE Bearing in mind that, in particular, the T666M mutation contributes to a large proportion of FHM linked to chromosome 19, we conclude that common migraine is distinct from FHM in its molecular basis and, therefore, most likely also in its pathophysiology. 12705332

2003