rs2039381
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs2039381(C;C) |
| Make rs2039381(C;T) |
| Make rs2039381(T;T) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 9 |
| Position | 21481484 |
| Gene | IFNE, MIR31HG |
| is a | snp |
| is | mentioned by |
| dbSNP | rs2039381 |
| dbSNP (classic) | rs2039381 |
| ClinGen | rs2039381 |
| ebi | rs2039381 |
| HLI | rs2039381 |
| Exac | rs2039381 |
| Gnomad | rs2039381 |
| Varsome | rs2039381 |
| LitVar | rs2039381 |
| Map | rs2039381 |
| PheGenI | rs2039381 |
| Biobank | rs2039381 |
| 1000 genomes | rs2039381 |
| hgdp | rs2039381 |
| ensembl | rs2039381 |
| geneview | rs2039381 |
| scholar | rs2039381 |
| rs2039381 | |
| pharmgkb | rs2039381 |
| gwascentral | rs2039381 |
| openSNP | rs2039381 |
| 23andMe | rs2039381 |
| SNPshot | rs2039381 |
| SNPdbe | rs2039381 |
| MSV3d | rs2039381 |
| GWAS Ctlg | rs2039381 |
| GMAF | 0.06474 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 23802172] Association study between nonsense polymorphism (rs2039381, Gln71Stop) of Interferon-ε and susceptibility to vitiligo in Korean population
[PMID 24055696] T Allele of Nonsense Polymorphism (rs2039381, Gln71Stop) of Interferon-ε is a Risk Factor for the Development of Intracerebral Hemorrhage
