rs4762767
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs4762767(C;C) |
| Make rs4762767(C;T) |
| Make rs4762767(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 12 |
| Position | 19713195 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs4762767 |
| dbSNP (classic) | rs4762767 |
| ClinGen | rs4762767 |
| ebi | rs4762767 |
| HLI | rs4762767 |
| Exac | rs4762767 |
| Gnomad | rs4762767 |
| Varsome | rs4762767 |
| LitVar | rs4762767 |
| Map | rs4762767 |
| PheGenI | rs4762767 |
| Biobank | rs4762767 |
| 1000 genomes | rs4762767 |
| hgdp | rs4762767 |
| ensembl | rs4762767 |
| geneview | rs4762767 |
| scholar | rs4762767 |
| rs4762767 | |
| pharmgkb | rs4762767 |
| gwascentral | rs4762767 |
| openSNP | rs4762767 |
| 23andMe | rs4762767 |
| SNPshot | rs4762767 |
| SNPdbe | rs4762767 |
| MSV3d | rs4762767 |
| GWAS Ctlg | rs4762767 |
| GMAF | 0.3274 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 21946350 ]
|
| Trait | |
| Title | Genome-wide association and large-scale follow up identifies 16 new loci influencing lung function. |
| Risk Allele | G |
| P-val | 0.000008 |
| Odds Ratio | 0.0270 [0.015-0.039] unit decrease |
