{{Rsnum
|rsid=1800790
|Gene=FGB
|Chromosome=4
|position=154562556
|Orientation=plus
|GMAF=0.1598
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=FGB
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 3.5 | 45.6 | 50.9
| HCB | 0.0 | 0.0 | 0.0
| JPT | 0.0 | 0.0 | 0.0
| YRI | 0.0 | 0.0 | 0.0
| ASW | 0.0 | 0.0 | 0.0
| CHB | 0.0 | 0.0 | 0.0
| CHD | 0.0 | 0.0 | 0.0
| GIH | 0.0 | 0.0 | 0.0
| LWK | 0.0 | 0.0 | 0.0
| MEX | 0.0 | 0.0 | 0.0
| MKK | 0.0 | 0.0 | 0.0
| TSI | 0.0 | 0.0 | 0.0
| HapMapRevision=28
}}
{{PMID Auto
|PMID=19332210
|Title=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
|OA=1
}}
{{PMID Auto
|PMID=19136375
|Title=Fibrinogen genes modify the fibrinogen response to ambient particulate matter
}}

{{PMID Auto
|PMID=20167083
|Title=Fibrinogen beta variants confer protection against coronary artery disease in a Greek case-control study
|OA=1
}}

{{PMID Auto
|PMID=21291465
|Title=The association of genetic polymorphisms with cerebral palsy: a meta-analysis
}}

{{PMID Auto
|PMID=21332313
|Title=Sequence variations in the FII, FV, F13A1, FGB and PAI-1 genes are associated with differences in myocardial perfusion
}}

{{PMID Auto
|PMID=22386478
|Title=Fibrinogen polymorphisms associated with sporadic cerebral hemorrhage in a Chinese population
}}

{{PMID Auto
|PMID=18513389
|Title=New application of intelligent agents in sporadic amyotrophic lateral sclerosis identifies unexpected specific genetic background.
|OA=1
}}

{{PMID Auto
|PMID=18936436
|Title=Prevalence in the United States of selected candidate gene variants: Third National Health and Nutrition Examination Survey, 1991-1994.
|OA=1
}}

{{PMID Auto
|PMID=19131662
|Title=A meta-analysis of candidate gene polymorphisms and ischemic stroke in 6 study populations: association of lymphotoxin-alpha in nonhypertensive patients.
|OA=1
}}

{{PMID Auto
|PMID=19330901
|Title=Association of 77 polymorphisms in 52 candidate genes with blood pressure progression and incident hypertension: the Women's Genome Health Study.
|OA=1
}}

{{PMID Auto
|PMID=19559392
|Title=A candidate gene association study of 77 polymorphisms in migraine.
|OA=1
}}

{{PMID Auto
|PMID=19750100
|Title=Modification of the interleukin-6 response to air pollution by interleukin-6 and fibrinogen polymorphisms.
|OA=1
}}

{{PMID Auto
|PMID=20031576
|Title=Association of novel genetic Loci with circulating fibrinogen levels: a genome-wide association study in 6 population-based cohorts.
|OA=1
}}

{{PMID Auto
|PMID=20031577
|Title=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.
|OA=1
}}

{{PMID Auto
|PMID=20059469
|Title=Interaction between fibrinogen and IL-6 genetic variants and associations with cardiovascular disease risk in the Cardiovascular Health Study.
|OA=1
}}

{{PMID Auto
|PMID=22267327
|Title=Fibrinogen and factor XIII A-subunit genotypes interactively influence C-reactive protein levels during inflammation.
}}

{{PMID Auto
|PMID=22388766
|Title=A genetic instrument for Mendelian randomization of fibrinogen.
}}

{{PMID Auto
|PMID=23220916
|Title=Elevated fibrinogen levels are associated with risk of pulmonary embolism, but not with deep venous thrombosis.
}}

{{PMID Auto
|PMID=23274712
|Title=Genetic polymorphisms and the risk of myocardial infarction in patients under 45 years of age.
|OA=1
}}

{{PMID Auto
|PMID=23944290
|Title=Association between two functional fibrinogen-related polymorphisms and ischemic stroke: a case-control study
}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}