Source: GWASDB

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs10034922
rs10034922
CUI: C1561955
Disease: Fibrinogen, CTCAE
Fibrinogen, CTCAE 		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: rs10157379
rs10157379
NLRP3
CUI: C1561955
Disease: Fibrinogen, CTCAE
Fibrinogen, CTCAE 		T 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: rs1016988
rs1016988
CUI: C1561955
Disease: Fibrinogen, CTCAE
Fibrinogen, CTCAE 		G 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
dbSNP: rs10226084
rs10226084
CUI: C1561955
Disease: Fibrinogen, CTCAE
Fibrinogen, CTCAE 		T 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: rs1047891
rs1047891
CPS1
CUI: C1561955
Disease: Fibrinogen, CTCAE
Fibrinogen, CTCAE 		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
dbSNP: rs10512597
rs10512597
CD300LF ; RAB37
CUI: C1561955
Disease: Fibrinogen, CTCAE
Fibrinogen, CTCAE 		T 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: rs10512597
rs10512597
CD300LF ; RAB37
CUI: C1561955
Disease: Fibrinogen, CTCAE
Fibrinogen, CTCAE 		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
dbSNP: rs11242111
rs11242111
IRF1-AS1 ; LINC02863
CUI: C1561955
Disease: Fibrinogen, CTCAE
Fibrinogen, CTCAE 		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: rs1154988
rs1154988
CUI: C1561955
Disease: Fibrinogen, CTCAE
Fibrinogen, CTCAE 		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: rs12239046
rs12239046
NLRP3
CUI: C1561955
Disease: Fibrinogen, CTCAE
Fibrinogen, CTCAE 		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: rs12511469
rs12511469
CUI: C1561955
Disease: Fibrinogen, CTCAE
Fibrinogen, CTCAE 		A 0.700 GeneticVariation GWASDB Assessment of genetic determinants of the association of γ' fibrinogen in relation to cardiovascular disease. 21757653

2011
dbSNP: rs12651106
rs12651106
DCHS2
CUI: C1561955
Disease: Fibrinogen, CTCAE
Fibrinogen, CTCAE 		A 0.700 GeneticVariation GWASDB Assessment of genetic determinants of the association of γ' fibrinogen in relation to cardiovascular disease. 21757653

2011
dbSNP: rs12712127
rs12712127
IL1R1
CUI: C1561955
Disease: Fibrinogen, CTCAE
Fibrinogen, CTCAE 		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: rs12777
rs12777
SLC22A4 ; MIR3936HG
CUI: C1561955
Disease: Fibrinogen, CTCAE
Fibrinogen, CTCAE 		C 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
dbSNP: rs12915708
rs12915708
SPPL2A
CUI: C1561955
Disease: Fibrinogen, CTCAE
Fibrinogen, CTCAE 		C 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: rs1476698
rs1476698
FARP2
CUI: C1561955
Disease: Fibrinogen, CTCAE
Fibrinogen, CTCAE 		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: rs1539019
rs1539019
NLRP3
CUI: C1561955
Disease: Fibrinogen, CTCAE
Fibrinogen, CTCAE 		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: rs1539019
rs1539019
NLRP3
CUI: C1561955
Disease: Fibrinogen, CTCAE
Fibrinogen, CTCAE 		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: rs16844401
rs16844401
HGFAC
CUI: C1561955
Disease: Fibrinogen, CTCAE
Fibrinogen, CTCAE 		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: rs17690122
rs17690122
CUI: C1561955
Disease: Fibrinogen, CTCAE
Fibrinogen, CTCAE 		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: rs1800787
rs1800787
FGB
CUI: C1561955
Disease: Fibrinogen, CTCAE
Fibrinogen, CTCAE 		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
CUI: C1561955
Disease: Fibrinogen, CTCAE
Fibrinogen, CTCAE 		T 0.700 GeneticVariation GWASDB Assessment of genetic determinants of the association of γ' fibrinogen in relation to cardiovascular disease. 21757653

2011
dbSNP: rs1800789
rs1800789
FGB
CUI: C1561955
Disease: Fibrinogen, CTCAE
Fibrinogen, CTCAE 		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: rs1800789
rs1800789
FGB
CUI: C1561955
Disease: Fibrinogen, CTCAE
Fibrinogen, CTCAE 		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: rs1800790
rs1800790
FGB
CUI: C1561955
Disease: Fibrinogen, CTCAE
Fibrinogen, CTCAE 		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