Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1043994
rs1043994
NOTCH3
0.020 GeneticVariation BEFREE Altogether, 134 Finnish CADASIL patients with p.Arg133Cys mutation were analysed for possible associations between the apolipoprotein E (APOE) genotype, angiotensinogen (AGT) p.Met268Thr polymorphism or neutral p.Ala202Ala NOTCH3 polymorphism and earlier first-ever stroke or migraine. 25819272

2015
dbSNP: rs1043994
rs1043994
NOTCH3
0.020 GeneticVariation BEFREE However, association analysis revealed significant association of the single nucleotide polymorphism (SNP) rs1043994 with migraine. 16426270

2006