rs769258
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in complete genomics |
| Make rs769258(A;A) |
| Make rs769258(A;G) |
| Reference | GRCh37 37.1/131 |
| Chromosome | 22 |
| Position | 42130761 |
| Gene | CYP2D6, LOC102723722, LOC107987465, LOC107987481 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs769258 |
| dbSNP (classic) | rs769258 |
| ClinGen | rs769258 |
| ebi | rs769258 |
| HLI | rs769258 |
| Exac | rs769258 |
| Gnomad | rs769258 |
| Varsome | rs769258 |
| LitVar | rs769258 |
| Map | rs769258 |
| PheGenI | rs769258 |
| Biobank | rs769258 |
| 1000 genomes | rs769258 |
| hgdp | rs769258 |
| ensembl | rs769258 |
| geneview | rs769258 |
| scholar | rs769258 |
| rs769258 | |
| pharmgkb | rs769258 |
| gwascentral | rs769258 |
| openSNP | rs769258 |
| 23andMe | rs769258 |
| SNPshot | rs769258 |
| SNPdbe | rs769258 |
| MSV3d | rs769258 |
| GWAS Ctlg | rs769258 |
| GMAF | 0.02755 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
a variation in CYP2D6
[PMID 20070850
] Genome-wide association study confirms SNPs in SNCA and the MAPT region as common risk factors for Parkinson disease.
[PMID 23133420] Pharmacogenomic Diversity among Brazilians: Influence of Ancestry, Self-Reported Color, and Geographical Origin.
