rs77867647
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in complete genomics |
| Make rs77867647(A;A) |
| Make rs77867647(A;G) |
| Reference | GRCh37 37.1/131 |
| Chromosome | 22 |
| Position | 42127084 |
| Gene | CYP2D6, LOC102723722 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs77867647 |
| dbSNP (classic) | rs77867647 |
| ClinGen | rs77867647 |
| ebi | rs77867647 |
| HLI | rs77867647 |
| Exac | rs77867647 |
| Gnomad | rs77867647 |
| Varsome | rs77867647 |
| LitVar | rs77867647 |
| Map | rs77867647 |
| PheGenI | rs77867647 |
| Biobank | rs77867647 |
| 1000 genomes | rs77867647 |
| hgdp | rs77867647 |
| ensembl | rs77867647 |
| geneview | rs77867647 |
| scholar | rs77867647 |
| rs77867647 | |
| pharmgkb | rs77867647 |
| gwascentral | rs77867647 |
| openSNP | rs77867647 |
| 23andMe | rs77867647 |
| SNPshot | rs77867647 |
| SNPdbe | rs77867647 |
| MSV3d | rs77867647 |
| GWAS Ctlg | rs77867647 |
| Max Magnitude | 0 |
a variation in CYP2D6
