{{Rsnum
|rsid=443198
|Gene=NOTCH4
|Chromosome=6
|position=32222629
|Orientation=minus
|GMAF=0.4233
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=NOTCH4
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 10.6 | 47.8 | 41.6
| HCB | 27.2 | 47.8 | 25.0
| JPT | 36.0 | 43.2 | 20.7
| YRI | 21.1 | 42.2 | 36.7
| ASW | 17.5 | 43.9 | 38.6
| CHB | 27.2 | 47.8 | 25.0
| CHD | 31.5 | 43.5 | 25.0
| GIH | 28.6 | 48.0 | 23.5
| LWK | 20.0 | 50.0 | 30.0
| MEX | 20.7 | 39.7 | 39.7
| MKK | 34.0 | 47.4 | 18.6
| TSI | 12.7 | 50.0 | 37.3
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=21779181
|Trait=None
|Title=Identification of novel genetic markers associated with clinical phenotypes of systemic sclerosis through a genome-wide association strategy.
|RiskAllele=
|Pval=9E-21
|OR=1.8200
|ORtxt=[1.59-2.04]
|OA=1
}}

{{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}}