Rs1042157
From SNPedia
| Orientation | minus |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1042157 |
| PheGenI | rs1042157 |
| nextbio | rs1042157 |
| hapmap | rs1042157 |
| 1000 genomes | rs1042157 |
| hgdp | rs1042157 |
| ensembl | rs1042157 |
| gopubmed | rs1042157 |
| geneview | rs1042157 |
| scholar | rs1042157 |
| rs1042157 | |
| pharmgkb | rs1042157 |
| gwascentral | rs1042157 |
| openSNP | rs1042157 |
| 23andMe | rs1042157 |
| 23andMe all | rs1042157 |
| SNP Nexus | |
| SNPshot | rs1042157 |
| SNPdbe | rs1042157 |
| MSV3d | rs1042157 |
| Gene | SULT1A1 |
| Chromosome | 16 |
| Orientation | minus |
| GMAF | 0.2962 |
| Position | 28617057 |
| Reference | GRCh37 37.1/131 |
| Max Magnitude |
| Make rs1042157(C;C) |
| Make rs1042157(C;T) |
| Make rs1042157(T;T) |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
[PMID 20881232] Functional genetic variants in the 3'-untranslated region of sulfotransferase isoform 1A1 (SULT1A1) and their effect on enzymatic activity.
| GET Evidence | |
|---|---|
| rs1042157 | |
| aa_change | |
| aa_change_short | |
| impact | pharmacogenetic |
| qualified_impact | Insufficiently evaluated pharmacogenetic |
| overall_frequency | 0.242188 |
| summary | |