rs4148152
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs4148152(A;A) |
| Make rs4148152(A;G) |
| Make rs4148152(G;G) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 4 |
| Position | 88139757 |
| Gene | ABCG2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs4148152 |
| dbSNP (classic) | rs4148152 |
| ClinGen | rs4148152 |
| ebi | rs4148152 |
| HLI | rs4148152 |
| Exac | rs4148152 |
| Gnomad | rs4148152 |
| Varsome | rs4148152 |
| LitVar | rs4148152 |
| Map | rs4148152 |
| PheGenI | rs4148152 |
| Biobank | rs4148152 |
| 1000 genomes | rs4148152 |
| hgdp | rs4148152 |
| ensembl | rs4148152 |
| geneview | rs4148152 |
| scholar | rs4148152 |
| rs4148152 | |
| pharmgkb | rs4148152 |
| gwascentral | rs4148152 |
| openSNP | rs4148152 |
| 23andMe | rs4148152 |
| SNPshot | rs4148152 |
| SNPdbe | rs4148152 |
| MSV3d | rs4148152 |
| GWAS Ctlg | rs4148152 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 24513273 ]
|
| Trait | Serum uric acid levels |
| Title | A genome-wide association study identifies common variants influencing serum uric acid concentrations in a Chinese population. |
| Risk Allele | C |
| P-val | 3E-18 |
| Odds Ratio | .03 [0.021-0.037] unit decrease |
[PMID 25634581] Associations of the uric acid related genetic variants in SLC2A9 and ABCG2 loci with coronary heart disease risk
