rs4996601
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in complete genomics |
| (T;T) | 0 |
| Make rs4996601(C;T) |
| Reference | GRCh37 37.1/131 |
| Chromosome | 22 |
| Position | 42524544 |
| Gene | CYP2D6 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs4996601 |
| dbSNP (classic) | rs4996601 |
| ClinGen | rs4996601 |
| ebi | rs4996601 |
| HLI | rs4996601 |
| Exac | rs4996601 |
| Gnomad | rs4996601 |
| Varsome | rs4996601 |
| LitVar | rs4996601 |
| Map | rs4996601 |
| PheGenI | rs4996601 |
| Biobank | rs4996601 |
| 1000 genomes | rs4996601 |
| hgdp | rs4996601 |
| ensembl | rs4996601 |
| geneview | rs4996601 |
| scholar | rs4996601 |
| rs4996601 | |
| pharmgkb | rs4996601 |
| gwascentral | rs4996601 |
| openSNP | rs4996601 |
| 23andMe | rs4996601 |
| SNPshot | rs4996601 |
| SNPdbe | rs4996601 |
| MSV3d | rs4996601 |
| GWAS Ctlg | rs4996601 |
| Status | Deleted |
| Max Magnitude | 0 |
a variation in CYP2D6
