rs16851720
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs16851720(A;A) |
| Make rs16851720(A;C) |
| Make rs16851720(C;C) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 3 |
| Position | 141744456 |
| Gene | RNF7 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs16851720 |
| dbSNP (classic) | rs16851720 |
| ClinGen | rs16851720 |
| ebi | rs16851720 |
| HLI | rs16851720 |
| Exac | rs16851720 |
| Gnomad | rs16851720 |
| Varsome | rs16851720 |
| LitVar | rs16851720 |
| Map | rs16851720 |
| PheGenI | rs16851720 |
| Biobank | rs16851720 |
| 1000 genomes | rs16851720 |
| hgdp | rs16851720 |
| ensembl | rs16851720 |
| geneview | rs16851720 |
| scholar | rs16851720 |
| rs16851720 | |
| pharmgkb | rs16851720 |
| gwascentral | rs16851720 |
| openSNP | rs16851720 |
| 23andMe | rs16851720 |
| SNPshot | rs16851720 |
| SNPdbe | rs16851720 |
| MSV3d | rs16851720 |
| GWAS Ctlg | rs16851720 |
| GMAF | 0.1846 |
| Max Magnitude | 0 |
| ? | (A;A) (A;C) (C;C) | 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 | C |
| P-val | 9E-9 |
| Odds Ratio | NR NR |
[PMID 28338112] PNPLA3 and RNF7 Gene Variants are Associated with the Risk of Developing Liver Fibrosis and Cirrhosis in an Eastern European Population.
