rs3093105
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs3093105(G;G) |
| Make rs3093105(G;T) |
| Make rs3093105(T;T) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 19 |
| Position | 15897578 |
| Gene | CYP4F2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs3093105 |
| dbSNP (classic) | rs3093105 |
| ClinGen | rs3093105 |
| ebi | rs3093105 |
| HLI | rs3093105 |
| Exac | rs3093105 |
| Gnomad | rs3093105 |
| Varsome | rs3093105 |
| LitVar | rs3093105 |
| Map | rs3093105 |
| PheGenI | rs3093105 |
| Biobank | rs3093105 |
| 1000 genomes | rs3093105 |
| hgdp | rs3093105 |
| ensembl | rs3093105 |
| geneview | rs3093105 |
| scholar | rs3093105 |
| rs3093105 | |
| pharmgkb | rs3093105 |
| gwascentral | rs3093105 |
| openSNP | rs3093105 |
| 23andMe | rs3093105 |
| SNPshot | rs3093105 |
| SNPdbe | rs3093105 |
| MSV3d | rs3093105 |
| GWAS Ctlg | rs3093105 |
| GMAF | 0.1566 |
| Max Magnitude | 0 |
| ? | (G;G) (G;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 19097922] A haplotype of the CYP4F2 gene associated with myocardial infarction in Japanese men.
[PMID 18235092
] Association of a functional cytochrome P450 4F2 haplotype with urinary 20-HETE and hypertension.
[PMID 18250228] CYP4F2 genetic variant alters required warfarin dose.
[PMID 18787519] A haplotype of the CYP4F2 gene is associated with cerebral infarction in Japanese men.
[PMID 18971550] Haplotype-based case-control study of the human CYP4F2 gene and essential hypertension in Japanese subjects.
[PMID 19957603] [Association on the haplotypes of CYP4F2 gene and myocardial infarction].
