rs915947
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in complete genomics |
| Make rs915947(C;T) |
| Make rs915947(T;T) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 22 |
| Position | 42140943 |
| Gene | CYP2D7 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs915947 |
| dbSNP (classic) | rs915947 |
| ClinGen | rs915947 |
| ebi | rs915947 |
| HLI | rs915947 |
| Exac | rs915947 |
| Gnomad | rs915947 |
| Varsome | rs915947 |
| LitVar | rs915947 |
| Map | rs915947 |
| PheGenI | rs915947 |
| Biobank | rs915947 |
| 1000 genomes | rs915947 |
| hgdp | rs915947 |
| ensembl | rs915947 |
| geneview | rs915947 |
| scholar | rs915947 |
| rs915947 | |
| pharmgkb | rs915947 |
| gwascentral | rs915947 |
| openSNP | rs915947 |
| 23andMe | rs915947 |
| SNPshot | rs915947 |
| SNPdbe | rs915947 |
| MSV3d | rs915947 |
| GWAS Ctlg | rs915947 |
| Max Magnitude | 0 |
a variation in CYP2D6
