{{Rsnum
|rsid=3815188
|Gene=NOTCH3
|Chromosome=19
|position=15192414
|Orientation=plus
|GMAF=0.2383
|Gene_s=NOTCH3
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 1.8 | 27.4 | 70.8
| HCB | 16.1 | 50.4 | 33.6
| JPT | 16.1 | 50.9 | 33.0
| YRI | 6.2 | 36.3 | 57.5
| ASW | 10.5 | 36.8 | 52.6
| CHB | 16.1 | 50.4 | 33.6
| CHD | 18.3 | 40.4 | 41.3
| GIH | 2.0 | 19.8 | 78.2
| LWK | 9.2 | 45.9 | 45.0
| MEX | 6.9 | 27.6 | 65.5
| MKK | 19.2 | 45.5 | 35.3
| TSI | 5.9 | 27.7 | 66.3
| HapMapRevision=28
}}{{PMID Auto
|PMID=24086431
|Title=NOTCH3 Variants and Risk of Ischemic Stroke
|OA=1
}}

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

{{PMID Auto
|PMID=22664156
|Title=Mutational and haplotype map of NOTCH3 in a cohort of Italian patients with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL).
}}

{{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 v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}