rs12169962
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in complete genomics |
| Make rs12169962(C;T) |
| Make rs12169962(T;T) |
| Reference | GRCh37 37.1/131 |
| Chromosome | 22 |
| Position | 42126310 |
| Gene | CYP2D6 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs12169962 |
| dbSNP (classic) | rs12169962 |
| ClinGen | rs12169962 |
| ebi | rs12169962 |
| HLI | rs12169962 |
| Exac | rs12169962 |
| Gnomad | rs12169962 |
| Varsome | rs12169962 |
| LitVar | rs12169962 |
| Map | rs12169962 |
| PheGenI | rs12169962 |
| Biobank | rs12169962 |
| 1000 genomes | rs12169962 |
| hgdp | rs12169962 |
| ensembl | rs12169962 |
| geneview | rs12169962 |
| scholar | rs12169962 |
| rs12169962 | |
| pharmgkb | rs12169962 |
| gwascentral | rs12169962 |
| openSNP | rs12169962 |
| 23andMe | rs12169962 |
| SNPshot | rs12169962 |
| SNPdbe | rs12169962 |
| MSV3d | rs12169962 |
| GWAS Ctlg | rs12169962 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
a variation in CYP2D6
