rs2504916
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs2504916(A;A) |
| Make rs2504916(A;T) |
| Make rs2504916(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 6 |
| Position | 160402996 |
| Gene | SLC22A3 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs2504916 |
| dbSNP (classic) | rs2504916 |
| ClinGen | rs2504916 |
| ebi | rs2504916 |
| HLI | rs2504916 |
| Exac | rs2504916 |
| Gnomad | rs2504916 |
| Varsome | rs2504916 |
| LitVar | rs2504916 |
| Map | rs2504916 |
| PheGenI | rs2504916 |
| Biobank | rs2504916 |
| 1000 genomes | rs2504916 |
| hgdp | rs2504916 |
| ensembl | rs2504916 |
| geneview | rs2504916 |
| scholar | rs2504916 |
| rs2504916 | |
| pharmgkb | rs2504916 |
| gwascentral | rs2504916 |
| openSNP | rs2504916 |
| 23andMe | rs2504916 |
| SNPshot | rs2504916 |
| SNPdbe | rs2504916 |
| MSV3d | rs2504916 |
| GWAS Ctlg | rs2504916 |
| GMAF | 0.1515 |
| Max Magnitude | 0 |
| ? | (A;A) (A;T) (T;T) | 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 | T |
| P-val | 0.000002 |
| Odds Ratio | 0.3060 None |
