rs6841581

This variant is located in the EDNRA gene.

GWAS Catalog Trait Associations (6)

Genome-wide significant associations (p < 5×10⁻⁸) from the NHGRI-EBI GWAS Catalog.

coronary artery disease

Allele A
OR 1.08
p 3.0e-30
N 1,165,690
Large GWAS
European, NR
Allele A
OR 0.08
p 5.0e-24
N 547,261
Large GWAS
Verma A et al. Diversity and scale: Genetic architecture of 2068 traits in the VA Million Veteran Program. Science (new York, N.y.) 385(6706):eadj1182 (2024)
Allele A
OR 0.07
p 1.0e-13
N 404,034
Major Consortium StudyLarge GWAS
multi-ancestry
Allele A
OR 1.07
p 5.0e-10
N 63,731
Large GWAS
European, NR

brain aneurysm

Allele A
OR 0.22
p 3.0e-26
N 317,636
Large GWAS
multi-ancestry

heart failure

Allele A
OR 0.03
p 1.0e-8
N 2,358,556
Large GWAS
multi-ancestry

atherosclerosis

Verma A et al. Diversity and scale: Genetic architecture of 2068 traits in the VA Million Veteran Program. Science (new York, N.y.) 385(6706):eadj1182 (2024)
Allele G
OR 0.11
p 2.0e-13
N 615,003
Major Consortium StudyLarge GWAS
multi-ancestry

drug use measurement, coronary artery disease

Verma A et al. Diversity and scale: Genetic architecture of 2068 traits in the VA Million Veteran Program. Science (new York, N.y.) 385(6706):eadj1182 (2024)
Allele G
OR 0.07
p 3.0e-12
N 315,668
Major Consortium StudyLarge GWAS
European

myocardial infarction

Hartiala JA et al. Genome-wide analysis identifies novel susceptibility loci for myocardial infarction. European Heart Journal 42(9):919-933 (2021)
Allele A
OR 1.07
p 3.0e-10
N 639,221
Large GWAS
multi-ancestry

About EDNRA

This gene encodes the receptor for endothelin-1, a peptide that plays a role in potent and long-lasting vasoconstriction. This receptor associates with guanine-nucleotide-binding (G) proteins, and this coupling activates a phosphatidylinositol-calcium second messenger system. Polymorphisms in this gene have been linked to migraine headache resistance. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Oct 2009]

View all EDNRA variants →

Gene information from NCBI Gene. Variant classifications from ClinVar.

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