rs3024998
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs3024998(C;C) |
| Make rs3024998(C;T) |
| Make rs3024998(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 6 |
| Position | 43777840 |
| Gene | VEGFA |
| is a | snp |
| is | mentioned by |
| dbSNP | rs3024998 |
| dbSNP (classic) | rs3024998 |
| ClinGen | rs3024998 |
| ebi | rs3024998 |
| HLI | rs3024998 |
| Exac | rs3024998 |
| Gnomad | rs3024998 |
| Varsome | rs3024998 |
| LitVar | rs3024998 |
| Map | rs3024998 |
| PheGenI | rs3024998 |
| Biobank | rs3024998 |
| 1000 genomes | rs3024998 |
| hgdp | rs3024998 |
| ensembl | rs3024998 |
| geneview | rs3024998 |
| scholar | rs3024998 |
| rs3024998 | |
| pharmgkb | rs3024998 |
| gwascentral | rs3024998 |
| openSNP | rs3024998 |
| 23andMe | rs3024998 |
| SNPshot | rs3024998 |
| SNPdbe | rs3024998 |
| MSV3d | rs3024998 |
| GWAS Ctlg | rs3024998 |
| GMAF | 0.3499 |
| Max Magnitude | 0 |
[PMID 23211130] Polymorphisms in the vascular endothelial growth factor gene associated with recurrent spontaneous miscarriage
[PMID 17319747
] Large-scale evaluation of candidate genes identifies associations between VEGF polymorphisms and bladder cancer risk.
[PMID 21347390] Genetics of VEGF serum variation in human isolated populations of cilento: importance of VEGF polymorphisms.
