rs79292917
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (A;G) | 1.2 | CYP2D6 splice defect causing reduced function |
| (G;G) | 0 | common in complete genomics |
| Make rs79292917(A;A) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 22 |
| Position | 42127852 |
| Gene | CYP2D6, LOC102723722 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs79292917 |
| dbSNP (classic) | rs79292917 |
| ClinGen | rs79292917 |
| ebi | rs79292917 |
| HLI | rs79292917 |
| Exac | rs79292917 |
| Gnomad | rs79292917 |
| Varsome | rs79292917 |
| LitVar | rs79292917 |
| Map | rs79292917 |
| PheGenI | rs79292917 |
| Biobank | rs79292917 |
| 1000 genomes | rs79292917 |
| hgdp | rs79292917 |
| ensembl | rs79292917 |
| geneview | rs79292917 |
| scholar | rs79292917 |
| rs79292917 | |
| pharmgkb | rs79292917 |
| gwascentral | rs79292917 |
| openSNP | rs79292917 |
| 23andMe | rs79292917 |
| SNPshot | rs79292917 |
| SNPdbe | rs79292917 |
| MSV3d | rs79292917 |
| GWAS Ctlg | rs79292917 |
| Max Magnitude | 1.2 |
a variation in CYP2D6
