Gene: FGB ×
Source: GWASDB ×
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1800789
rs1800789
FGB
A 0.700 GeneticVariation GWASDB Multiethnic meta-analysis of genome-wide association studies in >100 000 subjects identifies 23 fibrinogen-associated Loci but no strong evidence of a causal association between circulating fibrinogen and cardiovascular disease. 23969696

2013
dbSNP: rs1800787
rs1800787
FGB
0.700 GeneticVariation GWASDB Common fibrinogen gene single nucleotide polymorphisms (FGB rs1800787 and FGG rs2066861) significantly associated with fibrinogen in EAs were prevalent in AAs and showed consistent associations. 20978265

2011
dbSNP: rs1800788
rs1800788
FGB
T 0.700 GeneticVariation GWASDB Assessment of genetic determinants of the association of γ' fibrinogen in relation to cardiovascular disease. 21757653

2011
dbSNP: rs1800790
rs1800790
FGB
0.700 GeneticVariation GWASDB Association of genomic loci from a cardiovascular gene SNP array with fibrinogen levels in European Americans and African-Americans from six cohort studies: the Candidate Gene Association Resource (CARe). 20978265

2011
dbSNP: rs2059503
rs2059503
FGB
0.700 GeneticVariation GWASDB Association of genomic loci from a cardiovascular gene SNP array with fibrinogen levels in European Americans and African-Americans from six cohort studies: the Candidate Gene Association Resource (CARe). 20978265

2011
dbSNP: rs2227421
rs2227421
FGB
0.700 GeneticVariation GWASDB Association of genomic loci from a cardiovascular gene SNP array with fibrinogen levels in European Americans and African-Americans from six cohort studies: the Candidate Gene Association Resource (CARe). 20978265

2011
dbSNP: rs4220
rs4220
FGB
0.700 GeneticVariation GWASDB Association of genomic loci from a cardiovascular gene SNP array with fibrinogen levels in European Americans and African-Americans from six cohort studies: the Candidate Gene Association Resource (CARe). 20978265

2011
dbSNP: rs6054
rs6054
FGB
0.700 GeneticVariation GWASDB We identified a rare Pro265Leu variant in FGB (rs6054) associated with lower fibrinogen. 20978265

2011
dbSNP: rs6056
rs6056
FGB
0.700 GeneticVariation GWASDB Association of genomic loci from a cardiovascular gene SNP array with fibrinogen levels in European Americans and African-Americans from six cohort studies: the Candidate Gene Association Resource (CARe). 20978265

2011
dbSNP: rs6058
rs6058
FGB
0.700 GeneticVariation GWASDB Association of genomic loci from a cardiovascular gene SNP array with fibrinogen levels in European Americans and African-Americans from six cohort studies: the Candidate Gene Association Resource (CARe). 20978265

2011
dbSNP: rs1800789
rs1800789
FGB
A 0.700 GeneticVariation GWASDB Association of novel genetic Loci with circulating fibrinogen levels: a genome-wide association study in 6 population-based cohorts. 20031576

2009
dbSNP: rs6056
rs6056
FGB
A 0.700 GeneticVariation GWASDB 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. 20031577

2009