Gene: NOTCH3 ×
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
dbSNP: rs137852642
rs137852642
NOTCH3
0.010 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: rs779558160
rs779558160
NOTCH3
0.010 GeneticVariation BEFREE The first part of the study, in a population of 275 migraineurs and 275 control individuals, found a significant association between the C381T variant and migraine, specifically in migraine without aura (MO) sufferers. 20813781

2011