G1691A
G1691A · SaudiVarKB evidence summary derived from retained literature mentions.
5Variant mentions
5Publications
2Associated gene records
2Associated phenotype records
Associated gene records
Co-mentioned in the same publicationsAssociated phenotype records
Co-mentioned in the same publications| Phenotype | Identifier / context | Articles | Mentions |
|---|---|---|---|
| stroke | — | 3 | 3 |
| sickle cell disease | HP:0001878 · 603903 | 1 | 1 |
Associated population records
Co-mentioned in the same publications| Population | Identifier / context | Articles | Mentions |
|---|---|---|---|
| Saudi Arabia | — | 1 | 1 |
| Population record | Cohort 100 | 1 | 1 |
| Population record | Cohort 6,860 | 1 | 1 |
| Saudi Arabia | Cohort 482 | 1 | 1 |
Supporting publications
5 records- 2025Screening of Factor V Leiden mutation and activated protein C resistance in Sudanese children with sickle cell disease and stroke: A descriptive cross-sectional study.Medicine1 mentions
- 2021The prevalence of Factor V Leiden (Arg506Gln) mutation in King Khalid University Hospital patients, 2017-2019.Nagoya journal of medical science1 mentions
- 2018Association between Factor V Gene Polymorphism and Risk of Ischemic Stroke: An Updated Meta-Analysis.Journal of stroke and cerebrovascular diseases : the official journal of National Stroke Association1 mentions
- 2016Molecular characterization of novel splice site mutation causing protein C deficiency.Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis1 mentions
- 2011Cerebral venous thrombosis associated with homozygous factor V Leiden mutation in a 15-year-old girl of Tunisian origin.Annals of Saudi medicine1 mentions