rs117791180
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs117791180(C;C) |
| Make rs117791180(C;T) |
| Make rs117791180(T;T) |
| Reference | GRCh38.p7 38.3/151 |
| Chromosome | 17 |
| Position | 46930382 |
| Gene | GOSR2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs117791180 |
| dbSNP (classic) | rs117791180 |
| ClinGen | rs117791180 |
| ebi | rs117791180 |
| HLI | rs117791180 |
| Exac | rs117791180 |
| Gnomad | rs117791180 |
| Varsome | rs117791180 |
| LitVar | rs117791180 |
| Map | rs117791180 |
| PheGenI | rs117791180 |
| Biobank | rs117791180 |
| 1000 genomes | rs117791180 |
| hgdp | rs117791180 |
| ensembl | rs117791180 |
| geneview | rs117791180 |
| scholar | rs117791180 |
| rs117791180 | |
| pharmgkb | rs117791180 |
| gwascentral | rs117791180 |
| openSNP | rs117791180 |
| 23andMe | rs117791180 |
| SNPshot | rs117791180 |
| SNPdbe | rs117791180 |
| MSV3d | rs117791180 |
| GWAS Ctlg | rs117791180 |
| Max Magnitude | 0 |
| GWAS snp | |
|---|---|
| PMID | [PMID 29066090 ]
|
| Trait | Idiopathic pulmonary fibrosis |
| Title | Genetic variants associated with susceptibility to idiopathic pulmonary fibrosis in people of European ancestry: a genome-wide association study. |
| Risk Allele | |
| P-val | |
| Odds Ratio | |
