Rs2844682
From SNPedia
| Orientation | minus |
| is a | snp |
| is | mentioned by |
| dbSNP | rs2844682 |
| PheGenI | rs2844682 |
| nextbio | rs2844682 |
| hapmap | rs2844682 |
| 1000 genomes | rs2844682 |
| hgdp | rs2844682 |
| ensembl | rs2844682 |
| gopubmed | rs2844682 |
| geneview | rs2844682 |
| scholar | rs2844682 |
| rs2844682 | |
| pharmgkb | rs2844682 |
| gwascentral | rs2844682 |
| openSNP | rs2844682 |
| 23andMe | rs2844682 |
| 23andMe all | rs2844682 |
| SNP Nexus | |
| SNPshot | rs2844682 |
| SNPdbe | rs2844682 |
| MSV3d | rs2844682 |
| Chromosome | 6 |
| Orientation | minus |
| GMAF | 0.1516 |
| Position | 30946148 |
| Reference | GRCh37 37.1/131 |
| Max Magnitude | 3 |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in complete genomics |
| (T;T) | 3 |
| Make rs2844682(C;T) |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
Helps to identify HLA-B*1502
| GET Evidence | |
|---|---|
| rs2844682 | |
| aa_change | |
| aa_change_short | |
| impact | pharmacogenetic |
| qualified_impact | Insufficiently evaluated pharmacogenetic |
| overall_frequency | 0.164062 |
| summary | |
