rs1558139
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs1558139(A;A) |
| Make rs1558139(A;G) |
| Make rs1558139(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 19 |
| Position | 15886754 |
| Gene | CYP4F2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1558139 |
| dbSNP (classic) | rs1558139 |
| ClinGen | rs1558139 |
| ebi | rs1558139 |
| HLI | rs1558139 |
| Exac | rs1558139 |
| Gnomad | rs1558139 |
| Varsome | rs1558139 |
| LitVar | rs1558139 |
| Map | rs1558139 |
| PheGenI | rs1558139 |
| Biobank | rs1558139 |
| 1000 genomes | rs1558139 |
| hgdp | rs1558139 |
| ensembl | rs1558139 |
| geneview | rs1558139 |
| scholar | rs1558139 |
| rs1558139 | |
| pharmgkb | rs1558139 |
| gwascentral | rs1558139 |
| openSNP | rs1558139 |
| 23andMe | rs1558139 |
| SNPshot | rs1558139 |
| SNPdbe | rs1558139 |
| MSV3d | rs1558139 |
| GWAS Ctlg | rs1558139 |
| GMAF | 0.4293 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
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[PMID 18971550] rs1558139 might be a genetic marker for EH and the T-T-G haplotype might be a protective genetic marker for essential hypertension in Japanese men.
[PMID 19097922] A haplotype of the CYP4F2 gene associated with myocardial infarction in Japanese men.
[PMID 17903306
] Genome-wide association study of electrocardiographic and heart rate variability traits: the Framingham Heart Study.
[PMID 18787519] A haplotype of the CYP4F2 gene is associated with cerebral infarction in Japanese men.
[PMID 19957603] [Association on the haplotypes of CYP4F2 gene and myocardial infarction].
[PMID 29484037] A Novel Polymorphism in the Promoter of the CYP4A11 Gene Is Associated with Susceptibility to Coronary Artery Disease.
