rs10478694
From SNPedia
| Merged into | rs1800997 |
| Orientation | plus |
| Stabilized | plus |
| Make rs10478694(-;-) |
| Make rs10478694(-;A) |
| Make rs10478694(A;A) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 6 |
| Position | 12290496 |
| Gene | EDN1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs10478694 |
| dbSNP (classic) | rs10478694 |
| ClinGen | rs10478694 |
| ebi | rs10478694 |
| HLI | rs10478694 |
| Exac | rs10478694 |
| Gnomad | rs10478694 |
| Varsome | rs10478694 |
| LitVar | rs10478694 |
| Map | rs10478694 |
| PheGenI | rs10478694 |
| Biobank | rs10478694 |
| 1000 genomes | rs10478694 |
| hgdp | rs10478694 |
| ensembl | rs10478694 |
| geneview | rs10478694 |
| scholar | rs10478694 |
| rs10478694 | |
| pharmgkb | rs10478694 |
| gwascentral | rs10478694 |
| openSNP | rs10478694 |
| 23andMe | rs10478694 |
| SNPshot | rs10478694 |
| SNPdbe | rs10478694 |
| MSV3d | rs10478694 |
| GWAS Ctlg | rs10478694 |
| Status | Merged into rs1800997 |
| Max Magnitude | 0 |
[PMID 24747133] Association of Endothelin-1 Gene Polymorphisms with the Clinical Phenotype in Primary Nephrotic Syndrome of Children
