rs10738760
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs10738760(A;A) |
| Make rs10738760(A;G) |
| Make rs10738760(G;G) |
| Reference | GRCh37.p2 37.2/134 |
| Chromosome | 9 |
| Position | 2691186 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs10738760 |
| dbSNP (classic) | rs10738760 |
| ClinGen | rs10738760 |
| ebi | rs10738760 |
| HLI | rs10738760 |
| Exac | rs10738760 |
| Gnomad | rs10738760 |
| Varsome | rs10738760 |
| LitVar | rs10738760 |
| Map | rs10738760 |
| PheGenI | rs10738760 |
| Biobank | rs10738760 |
| 1000 genomes | rs10738760 |
| hgdp | rs10738760 |
| ensembl | rs10738760 |
| geneview | rs10738760 |
| scholar | rs10738760 |
| rs10738760 | |
| pharmgkb | rs10738760 |
| gwascentral | rs10738760 |
| openSNP | rs10738760 |
| 23andMe | rs10738760 |
| SNPshot | rs10738760 |
| SNPdbe | rs10738760 |
| MSV3d | rs10738760 |
| GWAS Ctlg | rs10738760 |
| GMAF | 0.433 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 21757650 ]
|
| Trait | |
| Title | Identification of cis- and trans-Acting Genetic Variants Explaining Up to Half the Variation in Circulating Vascular Endothelial Growth Factor Levels. |
| Risk Allele | A |
| P-val | 1E-39 |
| Odds Ratio | None None |
[PMID 23204297] A common variant highly associated with plasma VEGFA levels also contributes to the variation of both LDL-C and HDL-C
[PMID 28267147] VEGF-related polymorphisms identified by GWAS and risk for major depression.
[PMID 30579324] Vascular endothelial growth factor (VEGF)-related polymorphisms rs10738760 and rs6921438 are not risk factors for proliferative diabetic retinopathy (PDR) in patients with type 2 diabetes mellitus (T2DM).
