rs11725957
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in complete genomics |
| Make rs11725957(A;A) |
| Make rs11725957(A;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 4 |
| Position | 49060875 |
| Gene | CWH43 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs11725957 |
| dbSNP (classic) | rs11725957 |
| ClinGen | rs11725957 |
| ebi | rs11725957 |
| HLI | rs11725957 |
| Exac | rs11725957 |
| Gnomad | rs11725957 |
| Varsome | rs11725957 |
| LitVar | rs11725957 |
| Map | rs11725957 |
| PheGenI | rs11725957 |
| Biobank | rs11725957 |
| 1000 genomes | rs11725957 |
| hgdp | rs11725957 |
| ensembl | rs11725957 |
| geneview | rs11725957 |
| scholar | rs11725957 |
| rs11725957 | |
| pharmgkb | rs11725957 |
| gwascentral | rs11725957 |
| openSNP | rs11725957 |
| 23andMe | rs11725957 |
| SNPshot | rs11725957 |
| SNPdbe | rs11725957 |
| MSV3d | rs11725957 |
| GWAS Ctlg | rs11725957 |
| GMAF | 0.01561 |
| 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 | 0.000008 |
| Odds Ratio | 0.7270 None |
