{{Rsnum
|rsid=5369
|Gene=EDN1
|Chromosome=6
|position=12294025
|Orientation=plus
|GMAF=0.09871
|Gene_s=EDN1
|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 | 2.7 | 20.4 | 77.0
| HCB | 0.0 | 2.2 | 97.8
| JPT | 0.0 | 1.8 | 98.2
| YRI | 5.4 | 28.6 | 66.0
| ASW | 1.8 | 26.3 | 71.9
| CHB | 0.0 | 2.2 | 97.8
| CHD | 0.0 | 9.2 | 90.8
| GIH | 0.0 | 14.9 | 85.1
| LWK | 2.7 | 33.6 | 63.6
| MEX | 1.7 | 6.9 | 91.4
| MKK | 0.6 | 19.2 | 80.1
| TSI | 0.0 | 20.6 | 79.4
| HapMapRevision=28
}}{{PMID Auto
|PMID=24035903
|Title=The -974 C&gt;A (rs3087459) gene polymorphism in the endothelin gene (EDN1) is associated with risk of developing acute coronary syndrome in Mexican patients
}}

{{PMID Auto
|PMID=15784727
|Title=Association of klotho, bone morphogenic protein 6, and annexin A2 polymorphisms with sickle cell osteonecrosis.
|OA=1
}}

{{PMID Auto
|PMID=15942023
|Title=Genome amplification of single sperm using multiple displacement amplification.
|OA=1
}}

{{PMID Auto
|PMID=16642433
|Title=Polymorphism in maternal LRP8 gene is associated with fetal growth.
|OA=1
}}

{{PMID Auto
|PMID=19593725
|Title=Association of maternally inherited GNAS alleles with African-American male birth weight.
|OA=1
}}

{{PMID Auto
|PMID=20401335
|Title=Sickle Cell Disease in the Post Genomic Era: A Monogenic Disease with a Polygenic Phenotype.
|OA=1
}}

{{PMID Auto
|PMID=21767690
|Title=The impact of endothelin-1 genetic analysis and job strain on ambulatory blood pressure.
}}

{{on chip | 23andMe v2}}
{{on chip | FTDNA}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}