rs10158897
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs10158897(C;C) |
| Make rs10158897(C;T) |
| Make rs10158897(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 1 |
| Position | 62447248 |
| Gene | USP1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs10158897 |
| dbSNP (classic) | rs10158897 |
| ClinGen | rs10158897 |
| ebi | rs10158897 |
| HLI | rs10158897 |
| Exac | rs10158897 |
| Gnomad | rs10158897 |
| Varsome | rs10158897 |
| LitVar | rs10158897 |
| Map | rs10158897 |
| PheGenI | rs10158897 |
| Biobank | rs10158897 |
| 1000 genomes | rs10158897 |
| hgdp | rs10158897 |
| ensembl | rs10158897 |
| geneview | rs10158897 |
| scholar | rs10158897 |
| rs10158897 | |
| pharmgkb | rs10158897 |
| gwascentral | rs10158897 |
| openSNP | rs10158897 |
| 23andMe | rs10158897 |
| SNPshot | rs10158897 |
| SNPdbe | rs10158897 |
| MSV3d | rs10158897 |
| GWAS Ctlg | rs10158897 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 24386095 ]
|
| Trait | Lipid traits |
| Title | A genome wide association study identifies common variants associated with lipid levels in the Chinese population. |
| Risk Allele | T |
| P-val | 9E-6 |
| Odds Ratio | .02 mmol/L decrease |
