rs1800790
| Orientation | plus |
| Stabilized | plus |
| Make rs1800790(A;A) |
| Make rs1800790(A;G) |
| Make rs1800790(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 4 |
| Position | 154562556 |
| Gene | FGB |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1800790 |
| dbSNP (classic) | rs1800790 |
| ClinGen | rs1800790 |
| ebi | rs1800790 |
| HLI | rs1800790 |
| Exac | rs1800790 |
| Gnomad | rs1800790 |
| Varsome | rs1800790 |
| LitVar | rs1800790 |
| Map | rs1800790 |
| PheGenI | rs1800790 |
| Biobank | rs1800790 |
| 1000 genomes | rs1800790 |
| hgdp | rs1800790 |
| ensembl | rs1800790 |
| geneview | rs1800790 |
| scholar | rs1800790 |
| rs1800790 | |
| pharmgkb | rs1800790 |
| gwascentral | rs1800790 |
| openSNP | rs1800790 |
| 23andMe | rs1800790 |
| SNPshot | rs1800790 |
| SNPdbe | rs1800790 |
| MSV3d | rs1800790 |
| GWAS Ctlg | rs1800790 |
| GMAF | 0.1598 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
Also known as 455G/A beta Fibrinogen polymorphism. A is the risk allele according to the following paper:
[PMID 29235504
] The β-fibrinogen gene 455G/A polymorphism associated with cardioembolic stroke in atrial fibrillation with low CHA2DS2-VaSc score.
[PMID 19332210] Candidate genetic variants in the fibrinogen, methylenetetrahydrofolate reductase, and intercellular adhesion molecule-1 genes and plasma levels of fibrinogen, homocysteine, and intercellular adhesion molecule-1 among various race/ethnic groups: Data from the Women's Genome Health Study
[PMID 19136375] Fibrinogen genes modify the fibrinogen response to ambient particulate matter
[PMID 20167083] Fibrinogen beta variants confer protection against coronary artery disease in a Greek case-control study
[PMID 21291465] The association of genetic polymorphisms with cerebral palsy: a meta-analysis
[PMID 21332313] Sequence variations in the FII, FV, F13A1, FGB and PAI-1 genes are associated with differences in myocardial perfusion
[PMID 22386478] Fibrinogen polymorphisms associated with sporadic cerebral hemorrhage in a Chinese population
[PMID 18513389] New application of intelligent agents in sporadic amyotrophic lateral sclerosis identifies unexpected specific genetic background.
[PMID 18936436] Prevalence in the United States of selected candidate gene variants: Third National Health and Nutrition Examination Survey, 1991-1994.
[PMID 19131662] A meta-analysis of candidate gene polymorphisms and ischemic stroke in 6 study populations: association of lymphotoxin-alpha in nonhypertensive patients.
[PMID 19330901] Association of 77 polymorphisms in 52 candidate genes with blood pressure progression and incident hypertension: the Women's Genome Health Study.
[PMID 19559392] A candidate gene association study of 77 polymorphisms in migraine.
[PMID 19750100] Modification of the interleukin-6 response to air pollution by interleukin-6 and fibrinogen polymorphisms.
[PMID 20031576] Association of novel genetic Loci with circulating fibrinogen levels: a genome-wide association study in 6 population-based cohorts.
[PMID 20031577] Novel loci, including those related to Crohn disease, psoriasis, and inflammation, identified in a genome-wide association study of fibrinogen in 17 686 women: the Women's Genome Health Study.
[PMID 20059469] Interaction between fibrinogen and IL-6 genetic variants and associations with cardiovascular disease risk in the Cardiovascular Health Study.
[PMID 22267327] Fibrinogen and factor XIII A-subunit genotypes interactively influence C-reactive protein levels during inflammation.
[PMID 22388766] A genetic instrument for Mendelian randomization of fibrinogen.
[PMID 23220916] Elevated fibrinogen levels are associated with risk of pulmonary embolism, but not with deep venous thrombosis.
[PMID 23274712] Genetic polymorphisms and the risk of myocardial infarction in patients under 45 years of age.
[PMID 23944290] Association between two functional fibrinogen-related polymorphisms and ischemic stroke: a case-control study
[PMID 25862345] Genetic association between FXIII and β-fibrinogen genes and women with recurrent spontaneous abortion: a meta- analysis
[PMID 27277665] Genetic risk factors for restenosis after percutaneous coronary intervention in Kazakh population.
[PMID 32214403] Evaluation of single nucleotide polymorphisms in 6 candidate genes and carotid intima-media thickness in community-dwelling residents.
