rs1043994, NOTCH3

N. diseases: 7
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Migraine Disorders
CUI: C0149931
Disease: Migraine Disorders
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
Migraine Disorders
CUI: C0149931
Disease: Migraine Disorders
0.020 GeneticVariation BEFREE However, association analysis revealed significant association of the single nucleotide polymorphism (SNP) rs1043994 with migraine. 16426270 2006