rs2071942
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs2071942(A;A) |
| Make rs2071942(A;G) |
| Make rs2071942(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 6 |
| Position | 12294760 |
| Gene | EDN1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs2071942 |
| dbSNP (classic) | rs2071942 |
| ClinGen | rs2071942 |
| ebi | rs2071942 |
| HLI | rs2071942 |
| Exac | rs2071942 |
| Gnomad | rs2071942 |
| Varsome | rs2071942 |
| LitVar | rs2071942 |
| Map | rs2071942 |
| PheGenI | rs2071942 |
| Biobank | rs2071942 |
| 1000 genomes | rs2071942 |
| hgdp | rs2071942 |
| ensembl | rs2071942 |
| geneview | rs2071942 |
| scholar | rs2071942 |
| rs2071942 | |
| pharmgkb | rs2071942 |
| gwascentral | rs2071942 |
| openSNP | rs2071942 |
| 23andMe | rs2071942 |
| SNPshot | rs2071942 |
| SNPdbe | rs2071942 |
| MSV3d | rs2071942 |
| GWAS Ctlg | rs2071942 |
| GMAF | 0.208 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
[PMID 22609442] Polymorphisms of Genes related to Endothelial cells are associated with Primary Biliary Cirrhosis patients of Cretan origin
[PMID 17576235] The association between endothelin-1 gene polymorphisms and susceptibility to vitiligo in a Korean population.
[PMID 31981468
] Endothelin-1 rs9296344 associates with the susceptibility of childhood primary nephrotic syndrome.
