rs4980785
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs4980785(C;C) |
| Make rs4980785(C;T) |
| Make rs4980785(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 11 |
| Position | 69419726 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs4980785 |
| dbSNP (classic) | rs4980785 |
| ClinGen | rs4980785 |
| ebi | rs4980785 |
| HLI | rs4980785 |
| Exac | rs4980785 |
| Gnomad | rs4980785 |
| Varsome | rs4980785 |
| LitVar | rs4980785 |
| Map | rs4980785 |
| PheGenI | rs4980785 |
| Biobank | rs4980785 |
| 1000 genomes | rs4980785 |
| hgdp | rs4980785 |
| ensembl | rs4980785 |
| geneview | rs4980785 |
| scholar | rs4980785 |
| rs4980785 | |
| pharmgkb | rs4980785 |
| gwascentral | rs4980785 |
| openSNP | rs4980785 |
| 23andMe | rs4980785 |
| SNPshot | rs4980785 |
| SNPdbe | rs4980785 |
| MSV3d | rs4980785 |
| GWAS Ctlg | rs4980785 |
| GMAF | 0.4688 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 22010048 ]
|
| Trait | |
| Title | A genome-wide association study identifies a novel susceptibility locus for renal cell carcinoma on 12p11.23. |
| Risk Allele | |
| P-val | 0.000002 |
| Odds Ratio | None None |
