rs2629751
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs2629751(A;A) |
| Make rs2629751(A;G) |
| Make rs2629751(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 12 |
| Position | 104028030 |
| Gene | GLT8D2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs2629751 |
| dbSNP (classic) | rs2629751 |
| ClinGen | rs2629751 |
| ebi | rs2629751 |
| HLI | rs2629751 |
| Exac | rs2629751 |
| Gnomad | rs2629751 |
| Varsome | rs2629751 |
| LitVar | rs2629751 |
| Map | rs2629751 |
| PheGenI | rs2629751 |
| Biobank | rs2629751 |
| 1000 genomes | rs2629751 |
| hgdp | rs2629751 |
| ensembl | rs2629751 |
| geneview | rs2629751 |
| scholar | rs2629751 |
| rs2629751 | |
| pharmgkb | rs2629751 |
| gwascentral | rs2629751 |
| openSNP | rs2629751 |
| 23andMe | rs2629751 |
| SNPshot | rs2629751 |
| SNPdbe | rs2629751 |
| MSV3d | rs2629751 |
| GWAS Ctlg | rs2629751 |
| GMAF | 0.3421 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 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 | G |
| P-val | 1E-7 |
| Odds Ratio | NR NR |
