rs1058164
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs1058164(C;C) |
| Make rs1058164(C;G) |
| Make rs1058164(G;G) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 22 |
| Position | 42129130 |
| Gene | CYP2D6, LOC102723722, LOC107987465, LOC107987481 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1058164 |
| dbSNP (classic) | rs1058164 |
| ClinGen | rs1058164 |
| ebi | rs1058164 |
| HLI | rs1058164 |
| Exac | rs1058164 |
| Gnomad | rs1058164 |
| Varsome | rs1058164 |
| LitVar | rs1058164 |
| Map | rs1058164 |
| PheGenI | rs1058164 |
| Biobank | rs1058164 |
| 1000 genomes | rs1058164 |
| hgdp | rs1058164 |
| ensembl | rs1058164 |
| geneview | rs1058164 |
| scholar | rs1058164 |
| rs1058164 | |
| pharmgkb | rs1058164 |
| gwascentral | rs1058164 |
| openSNP | rs1058164 |
| 23andMe | rs1058164 |
| SNPshot | rs1058164 |
| SNPdbe | rs1058164 |
| MSV3d | rs1058164 |
| GWAS Ctlg | rs1058164 |
| Merged from | Rs61736911 |
| GMAF | 0.3898 |
| Max Magnitude | 0 |
The 1661G>C variation in CYP2D6. Involved in a number of decreased and non-functioning CYP2D6 variants. This SNP does not yet appear to be common in consumer tests.
[PMID 18698231
] Polymorphisms affecting gene transcription and mRNA processing in pharmacogenetic candidate genes: detection through allelic expression imbalance in human target tissues.
[PMID 23133420] Pharmacogenomic Diversity among Brazilians: Influence of Ancestry, Self-Reported Color, and Geographical Origin.
