{{Rsnum
|rsid=6056
|Gene=FGB
|Chromosome=4
|position=154567669
|Orientation=plus
|GMAF=0.1726
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=FGB
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 65.5 | 31.0 | 3.5
| HCB | 62.0 | 34.3 | 3.6
| JPT | 77.0 | 22.1 | 0.9
| YRI | 81.0 | 17.0 | 2.0
| ASW | 91.2 | 8.8 | 0.0
| CHB | 62.0 | 34.3 | 3.6
| CHD | 54.1 | 39.4 | 6.4
| GIH | 65.3 | 29.7 | 5.0
| LWK | 84.5 | 15.5 | 0.0
| MEX | 60.3 | 32.8 | 6.9
| MKK | 87.2 | 12.2 | 0.6
| TSI | 66.7 | 28.4 | 4.9
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=20031577
|Trait=Fibrinogen
|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
|RiskAllele=A
|Pval=8E-39
|OR=12.94
|ORtxt=[NR] mg/dl increase
|OA=1
}}

{{PMID Auto
|PMID=18464913
|Title=A genome-wide association study identifies protein quantitative trait loci (pQTLs).
|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
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}