{{Rsnum
|rsid=6841581
|Gene=EDNRA
|Chromosome=4
|position=147480038
|Orientation=plus
|GMAF=0.214
|Gene_s=EDNRA
|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 | 0.9 | 24.8 | 74.3
| HCB | 7.3 | 27.0 | 65.7
| JPT | 10.6 | 39.8 | 49.6
| YRI | 7.5 | 44.9 | 47.6
| ASW | 7.0 | 43.9 | 49.1
| CHB | 7.3 | 27.0 | 65.7
| CHD | 3.7 | 38.5 | 57.8
| GIH | 1.0 | 33.7 | 65.3
| LWK | 12.7 | 45.5 | 41.8
| MEX | 5.2 | 31.0 | 63.8
| MKK | 8.3 | 47.4 | 44.2
| TSI | 4.9 | 28.4 | 66.7
| HapMapRevision=28
}}{{PMID Auto
|PMID=22106312
|Title=Common variant near the endothelin receptor type A (EDNRA) gene is associated with intracranial aneurysm risk
|OA=1
}}
{{PMID Auto
|PMID=22286173
|Title=Genome-wide association study for intracranial aneurysm in Japanese population identifies three candidate susceptible loci and a functional genetic variant at EDNRA
}}

{{PMID Auto
|PMID=23733552
|Title=Genetic risk factors for intracranial aneurysms: a meta-analysis in more than 116,000 individuals.
|OA=1
}}

{{PMID Auto GWAS
  |PMID=24262325
  |Trait=Coronary artery disease or large artery stroke
  |Title=Shared genetic susceptibility to ischemic stroke and coronary artery disease: a genome-wide analysis of common variants.
  |RiskAllele=
  |Pval=2E-8
  |OR=NR
  |ORtxt=NR
  }}
{{on chip | Affy GenomeWide 6}}