G20210A
G20210A · SaudiVarKB evidence summary derived from retained literature mentions.
4Variant mentions
4Publications
1Associated gene records
7Associated phenotype records
Associated gene records
Co-mentioned in the same publications| Gene | Identifier / context | Articles | Mentions |
|---|---|---|---|
| MTHFR | HGNC:7436 | 4 | 4 |
Associated phenotype records
Co-mentioned in the same publications| Phenotype | Identifier / context | Articles | Mentions |
|---|---|---|---|
| coronary artery disease | — | 2 | 2 |
| obesity | HP:0001513 | 1 | 1 |
| hypertension | — | 1 | 1 |
| diabetes mellitus | — | 1 | 1 |
| sickle cell disease | HP:0001878 · 603903 | 1 | 1 |
| stroke | — | 1 | 1 |
| myocardial infarction | — | 1 | 1 |
Associated population records
Co-mentioned in the same publications| Population | Identifier / context | Articles | Mentions |
|---|---|---|---|
| Population record | Cohort 129 | 1 | 1 |
| Saudi Arabia | Cohort 105 | 1 | 1 |
| Population record | Cohort 96 | 1 | 1 |
Supporting publications
4 records- 2011Cerebral venous thrombosis associated with homozygous factor V Leiden mutation in a 15-year-old girl of Tunisian origin.Annals of Saudi medicine1 mentions
- 2008Thrombophilia in young patients with acute myocardial infarction.Saudi medical journal1 mentions
- 2004Factor V-Leiden, prothrombin G20210A, and MTHFR C677T mutations among patients with sickle cell disease in Eastern Saudi Arabia.American journal of hematology1 mentions
- 2004Factor V G1691A, prothrombin G20210A, and methylenetetrahydrofolate reductase [MTHFR] C677T gene polymorphism in angiographically documented coronary artery disease.Journal of thrombosis and thrombolysis1 mentions