{{Rsnum
|rsid=2071277
|Gene=NOTCH4
|Chromosome=6
|position=32203906
|Orientation=minus
|GMAF=0.4215
|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 | 31.9 | 46.0 | 22.1
| HCB | 40.9 | 42.3 | 16.8
| JPT | 24.8 | 53.1 | 22.1
| YRI | 41.1 | 45.2 | 13.7
| ASW | 47.4 | 38.6 | 14.0
| CHB | 40.9 | 42.3 | 16.8
| CHD | 29.6 | 50.0 | 20.4
| GIH | 8.9 | 45.5 | 45.5
| LWK | 41.3 | 48.6 | 10.1
| MEX | 46.6 | 43.1 | 10.3
| MKK | 19.2 | 49.4 | 31.4
| TSI | 19.6 | 45.1 | 35.3
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=22694956
|Trait=None
|Title=Genome-wide association study of age-related macular degeneration identifies associated variants in the TNXB-FKBPL-NOTCH4 region of chromosome 6p21.3.
|RiskAllele=C
|Pval=2E-11
|OR=1.3000
|ORtxt=None
|OA=1
}}

{{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}}