rs1143671
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs1143671(C;C) |
| Make rs1143671(C;T) |
| Make rs1143671(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 3 |
| Position | 121928439 |
| Gene | SLC15A2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1143671 |
| dbSNP (classic) | rs1143671 |
| ClinGen | rs1143671 |
| ebi | rs1143671 |
| HLI | rs1143671 |
| Exac | rs1143671 |
| Gnomad | rs1143671 |
| Varsome | rs1143671 |
| LitVar | rs1143671 |
| Map | rs1143671 |
| PheGenI | rs1143671 |
| Biobank | rs1143671 |
| 1000 genomes | rs1143671 |
| hgdp | rs1143671 |
| ensembl | rs1143671 |
| geneview | rs1143671 |
| scholar | rs1143671 |
| rs1143671 | |
| pharmgkb | rs1143671 |
| gwascentral | rs1143671 |
| openSNP | rs1143671 |
| 23andMe | rs1143671 |
| SNPshot | rs1143671 |
| SNPdbe | rs1143671 |
| MSV3d | rs1143671 |
| GWAS Ctlg | rs1143671 |
| GMAF | 0.4908 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 18698231
] Polymorphisms affecting gene transcription and mRNA processing in pharmacogenetic candidate genes: detection through allelic expression imbalance in human target tissues.
