{{Rsnum
|rsid=1043994
|Gene=NOTCH3
|Chromosome=19
|position=15192033
|Orientation=minus
|ReferenceAllele=A
|GMAF=0.1442
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=NOTCH3
}}A study of ~100 German patients suffering from [[migraines]] reported SNP [[rs1043994]] to be significantly associated with increased risk. {{PMID|16426270}}
{{ neighbor
| rsid = 28933697
| distance = 62
}}

{{PMID|22006983|OA=1
}} Genetic variants of the NOTCH3 gene in the elderly and magnetic resonance imaging correlates of age-related cerebral small vessel disease.

{{PMID|22373597}} Two novel mutations and a previously unreported intronic polymorphism in the NOTCH3 gene.

{{PMID Auto
|PMID=25120811
|Title=Notch1 single nucleotide polymorphism rs3124591 is associated with the risk of development of invasive ductal breast carcinoma in a Chinese population
}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | HumanOmni1Quad}}