{{Rsnum
|rsid=2066865
|Gene=FGG
|Chromosome=4
|position=154604124
|Orientation=minus
|GMAF=0.3186
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=FGG
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 60.7 | 33.9 | 5.4
| HCB | 23.7 | 51.1 | 25.2
| JPT | 25.9 | 53.6 | 20.5
| YRI | 44.4 | 47.2 | 8.3
| ASW | 42.1 | 47.4 | 10.5
| CHB | 23.7 | 51.1 | 25.2
| CHD | 25.9 | 50.9 | 23.1
| GIH | 58.4 | 33.7 | 7.9
| LWK | 42.1 | 45.8 | 12.1
| MEX | 62.1 | 36.2 | 1.7
| MKK | 54.2 | 38.7 | 7.1
| TSI | 60.4 | 34.7 | 5.0
| 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=20709368
|Title=The fibrinogen gamma 10034C&gt;T polymorphism is not associated with Peripheral Arterial Disease
}}

{{PMID Auto
|PMID=22707612
|Title=Genetic Risk Factors for Thrombosis in Systemic Lupus Erythematosus
|OA=1
}}

{{PMID|16144795}} Genetic variation in the fibrinogen gamma gene increases the risk for deep venous thrombosis by reducing plasma fibrinogen gamma' levels.

{{PMID|17445871}} The fibrinogen gamma (FGG) 10034C>T polymorphism is associated with venous thrombosis.

{{PMID|21422408}} Clotting factor gene polymorphisms and colorectal cancer risk.

{{PMID Auto
|PMID=23150947
|Title=Single nucleotide polymorphisms and the risk of venous thrombosis: results from a Danish case-cohort study
}}

{{PMID Auto
|PMID=25091233
|Title=Association of F11 polymorphism rs2289252 with deep vein thrombosis and related phenotypes in population of Latvia
}}

{{PMID Auto
|PMID=25210051
|Title=Genetic Variations Associated with Recurrent Venous Thrombosis
}}
{{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}}