{{Rsnum
|rsid=2070016
|Gene=FGA
|Chromosome=4
|position=154589162
|Orientation=minus
|GMAF=0.1341
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=FGA
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 1.8 | 27.9 | 70.3
| HCB | 2.9 | 33.1 | 64.0
| JPT | 0.9 | 27.4 | 71.7
| YRI | 0.0 | 4.8 | 95.2
| ASW | 1.8 | 12.3 | 86.0
| CHB | 2.9 | 33.1 | 64.0
| CHD | 7.4 | 36.1 | 56.5
| GIH | 2.0 | 20.8 | 77.2
| LWK | 0.0 | 3.7 | 96.3
| MEX | 0.0 | 26.3 | 73.7
| MKK | 0.0 | 7.1 | 92.9
| TSI | 3.0 | 28.7 | 68.3
| HapMapRevision=28
}}
{{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=19190816
|Title=Association study between variants in the fibrinogen gene cluster, fibrinogen levels and hypertension: results from the MONICA/KORA study.
}}

{{PMID Auto
|PMID=19552680
|Title=Common hemostasis and inflammation gene variants and venous thrombosis in older adults from the Cardiovascular Health Study.
|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
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | FTDNA}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}