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rs1049636

From SNPedia

Orientationminus
Stabilizedminus
Make rs1049636(C;C)
Make rs1049636(C;T)
Make rs1049636(T;T)
ReferenceGRCh38 38.1/141
Chromosome4
Position154604818
GeneFGG
is asnp
is mentioned by
dbSNPrs1049636
ebirs1049636
HLIrs1049636
Exacrs1049636
Varsomers1049636
Maprs1049636
PheGenIrs1049636
hapmaprs1049636
1000 genomesrs1049636
hgdprs1049636
ensemblrs1049636
gopubmedrs1049636
geneviewrs1049636
scholarrs1049636
googlers1049636
pharmgkbrs1049636
gwascentralrs1049636
openSNPrs1049636
23andMers1049636
23andMe allrs1049636
SNP Nexus

SNPshotrs1049636
SNPdbers1049636
MSV3drs1049636
GWAS Ctlgrs1049636
GMAF0.2736
Max Magnitude
? (C;C) (C;T) (T;T) 28
[PMID 21757653OA-icon.png] Assessment of genetic determinants of the association of (gamma)' fibrinogen in relation to cardiovascular disease


[PMID 16525568] Epistatic and pleiotropic effects of polymorphisms in the fibrinogen and coagulation factor XIII genes on plasma fibrinogen concentration, fibrin gel structure and risk of myocardial infarction.


[PMID 17241179] The association between fibrinogen haplotypes and myocardial infarction in men is partly mediated through pleiotropic effects on the serum IL-6 concentration.


[PMID 17263791] Elevated plasma fibrinogen gamma' concentration is associated with myocardial infarction: effects of variation in fibrinogen genes and environmental factors.


[PMID 18974842OA-icon.png] Gender differences in genetic risk profiles for cardiovascular disease.


[PMID 19190816] Association study between variants in the fibrinogen gene cluster, fibrinogen levels and hypertension: results from the MONICA/KORA study.


[PMID 20031577OA-icon.png] 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.