{{Rsnum
|rsid=3134931
|Gene=NOTCH4
|Chromosome=6
|position=32222843
|Orientation=minus
|GMAF=0.416
|Gene_s=NOTCH4
|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 | 48.7 | 41.6 | 9.7
| HCB | 18.2 | 54.0 | 27.7
| JPT | 25.7 | 37.2 | 37.2
| YRI | 32.0 | 47.6 | 20.4
| ASW | 22.8 | 52.6 | 24.6
| CHB | 18.2 | 54.0 | 27.7
| CHD | 22.0 | 36.7 | 41.3
| GIH | 36.6 | 42.6 | 20.8
| LWK | 32.7 | 47.3 | 20.0
| MEX | 34.5 | 48.3 | 17.2
| MKK | 32.1 | 43.6 | 24.4
| TSI | 45.1 | 47.1 | 7.8
| HapMapRevision=28
}}{{PMID Auto GWAS
  |PMID=23620142
  |Trait=Circulating myeloperoxidase levels (serum)
  |Title=Genome-wide and gene-centric analyses of circulating myeloperoxidase levels in the charge and care consortia.
  |RiskAllele=T
  |Pval=1E-8
  |OR=.05
  |ORtxt=[0.030-0.070] unit decrease
  }}

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