rs4149081
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs4149081(A;A) |
| Make rs4149081(A;G) |
| Make rs4149081(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 12 |
| Position | 21225087 |
| Gene | SLCO1B1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs4149081 |
| dbSNP (classic) | rs4149081 |
| ClinGen | rs4149081 |
| ebi | rs4149081 |
| HLI | rs4149081 |
| Exac | rs4149081 |
| Gnomad | rs4149081 |
| Varsome | rs4149081 |
| LitVar | rs4149081 |
| Map | rs4149081 |
| PheGenI | rs4149081 |
| Biobank | rs4149081 |
| 1000 genomes | rs4149081 |
| hgdp | rs4149081 |
| ensembl | rs4149081 |
| geneview | rs4149081 |
| scholar | rs4149081 |
| rs4149081 | |
| pharmgkb | rs4149081 |
| gwascentral | rs4149081 |
| openSNP | rs4149081 |
| 23andMe | rs4149081 |
| SNPshot | rs4149081 |
| SNPdbe | rs4149081 |
| MSV3d | rs4149081 |
| GWAS Ctlg | rs4149081 |
| GMAF | 0.2525 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
[PMID 19901119
] Germline Genetic Variation in an Organic Anion Transporter Polypeptide Associated With Methotrexate Pharmacokinetics and Clinical Effects
[PMID 21387541] Polymorphisms of the SLCO1B1 gene predict methotrexate-related toxicity in childhood acute lymphoblastic leukemia
| GWAS snp | |
|---|---|
| PMID | [PMID 21886157]
|
| Trait | |
| Title | Human metabolic individuality in biomedical and pharmaceutical research. |
| Risk Allele | A |
| P-val | 3E-22 |
| Odds Ratio | 0.2090 None |
[PMID 22668755] Intronic variants in SLCO1B1 related to statin-induced myopathy are associated with the low-density lipoprotein cholesterol response to statins in Chinese patients with hyperlipidaemia
