rs2189784
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs2189784(A;A) |
| Make rs2189784(A;G) |
| Make rs2189784(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 19 |
| Position | 15848390 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs2189784 |
| dbSNP (classic) | rs2189784 |
| ClinGen | rs2189784 |
| ebi | rs2189784 |
| HLI | rs2189784 |
| Exac | rs2189784 |
| Gnomad | rs2189784 |
| Varsome | rs2189784 |
| LitVar | rs2189784 |
| Map | rs2189784 |
| PheGenI | rs2189784 |
| Biobank | rs2189784 |
| 1000 genomes | rs2189784 |
| hgdp | rs2189784 |
| ensembl | rs2189784 |
| geneview | rs2189784 |
| scholar | rs2189784 |
| rs2189784 | |
| pharmgkb | rs2189784 |
| gwascentral | rs2189784 |
| openSNP | rs2189784 |
| 23andMe | rs2189784 |
| SNPshot | rs2189784 |
| SNPdbe | rs2189784 |
| MSV3d | rs2189784 |
| GWAS Ctlg | rs2189784 |
| GMAF | 0.3526 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
[PMID 19741565] Effects of CYP4F2 genetic polymorphisms and haplotypes on clinical outcomes in patients initiated on warfarin therapy
[PMID 20504253
] Combined CYP2C9, VKORC1 and CYP4F2 frequencies among racial and ethnic groups
[PMID 18535201] A genome-wide scan for common genetic variants with a large influence on warfarin maintenance dose.
