Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs886039322
rs886039322
Entrez Id: 773
Gene Symbol: CACNA1A
CACNA1A
CUI: C0149931
Disease:
Migraine Disorders
0.010 GeneticVariation BEFREE In conclusion we propose that rare variants in ATP1A2 are involved in the susceptibility to common forms of migraine, because of 1) the absence of alterations in controls, 2) the particular pattern of segregation in both families, 3) the high conservation of mutated residues in Na(+)/K(+)-ATPases, 4) the functional effect of C515Y, and 5) the involvement of ATP1A2 in a monogenic form of migraine. 16110494 2005