rs479200
From SNPedia
| Orientation | minus |
| Make rs479200(C;C) |
| Make rs479200(C;T) |
| Make rs479200(T;T) |
| Reference | GRCh38.p7 38.3/151 |
| Chromosome | 1 |
| Position | 231408034 |
| Gene | EGLN1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs479200 |
| dbSNP (classic) | rs479200 |
| ClinGen | rs479200 |
| ebi | rs479200 |
| HLI | rs479200 |
| Exac | rs479200 |
| Gnomad | rs479200 |
| Varsome | rs479200 |
| LitVar | rs479200 |
| Map | rs479200 |
| PheGenI | rs479200 |
| Biobank | rs479200 |
| 1000 genomes | rs479200 |
| hgdp | rs479200 |
| ensembl | rs479200 |
| geneview | rs479200 |
| scholar | rs479200 |
| rs479200 | |
| pharmgkb | rs479200 |
| gwascentral | rs479200 |
| openSNP | rs479200 |
| 23andMe | rs479200 |
| SNPshot | rs479200 |
| SNPdbe | rs479200 |
| MSV3d | rs479200 |
| GWAS Ctlg | rs479200 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 31009679] Novel association of SNP rs479200 in EGLN1 gene with predisposition to preeclampsia.
[PMID 32464411] Hypoxia responsiveness linked variant in EGLN1 gene is enriched in oral cancer patients.
