rs9380516
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs9380516(C;C) |
| Make rs9380516(C;T) |
| Make rs9380516(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 6 |
| Position | 35534425 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs9380516 |
| dbSNP (classic) | rs9380516 |
| ClinGen | rs9380516 |
| ebi | rs9380516 |
| HLI | rs9380516 |
| Exac | rs9380516 |
| Gnomad | rs9380516 |
| Varsome | rs9380516 |
| LitVar | rs9380516 |
| Map | rs9380516 |
| PheGenI | rs9380516 |
| Biobank | rs9380516 |
| 1000 genomes | rs9380516 |
| hgdp | rs9380516 |
| ensembl | rs9380516 |
| geneview | rs9380516 |
| scholar | rs9380516 |
| rs9380516 | |
| pharmgkb | rs9380516 |
| gwascentral | rs9380516 |
| openSNP | rs9380516 |
| 23andMe | rs9380516 |
| SNPshot | rs9380516 |
| SNPdbe | rs9380516 |
| MSV3d | rs9380516 |
| GWAS Ctlg | rs9380516 |
| GMAF | 0.1433 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 22841784 ]
|
| Trait | Hepatitis C induced liver fibrosis |
| Title | Genome-wide association study identifies variants associated with progression of liver fibrosis from HCV infection. |
| Risk Allele | T |
| P-val | 5E-7 |
| Odds Ratio | NR NR |
