rs833069
| Orientation | minus |
| Stabilized | minus |
| Make rs833069(A;A) |
| Make rs833069(A;G) |
| Make rs833069(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 6 |
| Position | 43774842 |
| Gene | VEGFA |
| is a | snp |
| is | mentioned by |
| dbSNP | rs833069 |
| dbSNP (classic) | rs833069 |
| ClinGen | rs833069 |
| ebi | rs833069 |
| HLI | rs833069 |
| Exac | rs833069 |
| Gnomad | rs833069 |
| Varsome | rs833069 |
| LitVar | rs833069 |
| Map | rs833069 |
| PheGenI | rs833069 |
| Biobank | rs833069 |
| 1000 genomes | rs833069 |
| hgdp | rs833069 |
| ensembl | rs833069 |
| geneview | rs833069 |
| scholar | rs833069 |
| rs833069 | |
| pharmgkb | rs833069 |
| gwascentral | rs833069 |
| openSNP | rs833069 |
| 23andMe | rs833069 |
| SNPshot | rs833069 |
| SNPdbe | rs833069 |
| MSV3d | rs833069 |
| GWAS Ctlg | rs833069 |
| GMAF | 0.4238 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
[PMID 20471686] Association of Age-related Macular Degeneration with Polymorphisms in Vascular Endothelial Growth Factor and Its Receptor
[PMID 21316969] Polymorphisms of the vascular endothelial growth factor A gene and susceptibility to sporadic brain arteriovenous malformation in a Chinese population
[PMID 22162628
] Polymorphisms in the vascular endothelial growth factor gene and the risk of diabetic retinopathy in Chinese patients with type 2 diabetes
[PMID 20018062] Identification of genes and haplotypes that predict rheumatoid arthritis using random forests.
[PMID 22307775] Polymorphisms in the VEGF-A in polypoidal choroidal vasculopathy in a Korean population.
[PMID 23211130] Polymorphisms in the vascular endothelial growth factor gene associated with recurrent spontaneous miscarriage
[PMID 23559864] Pharmacogenetic association with early response to intravitreal ranibizumab for age-related macular degeneration in a Korean population
[PMID 24652518] VEGFA and VEGFR2 gene polymorphisms and response to anti-vascular endothelial growth factor therapy: comparison of age-related macular degeneration treatments trials (CATT)
[PMID 24811984] Patient genotypes impact survival after surgery for isolated congenital heart disease
[PMID 31586488] Effect of gene polymorphisms in ADAM33, TGFβ1, VEGFA, and PLAUR on asthma in Thai population.
