rs6841581
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs6841581(A;A) |
Make rs6841581(A;G) |
Make rs6841581(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 4 |
Position | 147480038 |
Gene | EDNRA |
is a | snp |
is | mentioned by |
dbSNP | rs6841581 |
dbSNP (classic) | rs6841581 |
ClinGen | rs6841581 |
ebi | rs6841581 |
HLI | rs6841581 |
Exac | rs6841581 |
Gnomad | rs6841581 |
Varsome | rs6841581 |
LitVar | rs6841581 |
Map | rs6841581 |
PheGenI | rs6841581 |
Biobank | rs6841581 |
1000 genomes | rs6841581 |
hgdp | rs6841581 |
ensembl | rs6841581 |
geneview | rs6841581 |
scholar | rs6841581 |
rs6841581 | |
pharmgkb | rs6841581 |
gwascentral | rs6841581 |
openSNP | rs6841581 |
23andMe | rs6841581 |
SNPshot | rs6841581 |
SNPdbe | rs6841581 |
MSV3d | rs6841581 |
GWAS Ctlg | rs6841581 |
GMAF | 0.214 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 22106312] Common variant near the endothelin receptor type A (EDNRA) gene is associated with intracranial aneurysm risk
[PMID 22286173] Genome-wide association study for intracranial aneurysm in Japanese population identifies three candidate susceptible loci and a functional genetic variant at EDNRA
[PMID 23733552] Genetic risk factors for intracranial aneurysms: a meta-analysis in more than 116,000 individuals.
GWAS snp | |
---|---|
PMID | [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. |
Risk Allele | |
P-val | 2E-8 |
Odds Ratio | NR NR |
[PMID 26178354] [Association between genetic polymorphisms of EDNRA gene and high altitude polycythemia in Tibetans at the Qinghai-Tibetan Plateau]
[PMID 30823506] Genomic Variations in Susceptibility to Intracranial Aneurysm in the Korean Population.