rs10789491
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs10789491(A;A) |
| Make rs10789491(A;G) |
| Make rs10789491(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 1 |
| Position | 46713638 |
| Gene | EFCAB14 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs10789491 |
| dbSNP (classic) | rs10789491 |
| ClinGen | rs10789491 |
| ebi | rs10789491 |
| HLI | rs10789491 |
| Exac | rs10789491 |
| Gnomad | rs10789491 |
| Varsome | rs10789491 |
| LitVar | rs10789491 |
| Map | rs10789491 |
| PheGenI | rs10789491 |
| Biobank | rs10789491 |
| 1000 genomes | rs10789491 |
| hgdp | rs10789491 |
| ensembl | rs10789491 |
| geneview | rs10789491 |
| scholar | rs10789491 |
| rs10789491 | |
| pharmgkb | rs10789491 |
| gwascentral | rs10789491 |
| openSNP | rs10789491 |
| 23andMe | rs10789491 |
| SNPshot | rs10789491 |
| SNPdbe | rs10789491 |
| MSV3d | rs10789491 |
| GWAS Ctlg | rs10789491 |
| GMAF | 0.1446 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 22095909] |
| Trait | |
| Title | Serum ferritin levels are associated with a distinct phenotype of chronic hepatitis C poorly responding to pegylated interferon-alpha and ribavirin therapy. |
| Risk Allele | G |
| P-val | 0.000001 |
| Odds Ratio | 0.3120 None |
