Have questions? Visit https://www.reddit.com/r/SNPedia

rs1800790

From SNPedia

Orientationplus
Stabilizedplus
Make rs1800790(A;A)
Make rs1800790(A;G)
Make rs1800790(G;G)
ReferenceGRCh38 38.1/141
Chromosome4
Position154562556
GeneFGB
is asnp
is mentioned by
dbSNPrs1800790
ebirs1800790
HLIrs1800790
Exacrs1800790
Varsomers1800790
Maprs1800790
PheGenIrs1800790
hapmaprs1800790
1000 genomesrs1800790
hgdprs1800790
ensemblrs1800790
gopubmedrs1800790
geneviewrs1800790
scholarrs1800790
googlers1800790
pharmgkbrs1800790
gwascentralrs1800790
openSNPrs1800790
23andMers1800790
23andMe allrs1800790
SNP Nexus

SNPshotrs1800790
SNPdbers1800790
MSV3drs1800790
GWAS Ctlgrs1800790
GMAF0.1598
Max Magnitude
? (A;A) (A;G) (G;G) 28
[PMID 19332210OA-icon.png] Candidate genetic variants in the fibrinogen, methylenetetrahydrofolate reductase, and intercellular adhesion molecule-1 genes and plasma levels of fibrinogen, homocysteine, and intercellular adhesion molecule-1 among various race/ethnic groups: Data from the Women's Genome Health Study

[PMID 19136375] Fibrinogen genes modify the fibrinogen response to ambient particulate matter


[PMID 20167083OA-icon.png] Fibrinogen beta variants confer protection against coronary artery disease in a Greek case-control study


[PMID 21291465] The association of genetic polymorphisms with cerebral palsy: a meta-analysis


[PMID 21332313] Sequence variations in the FII, FV, F13A1, FGB and PAI-1 genes are associated with differences in myocardial perfusion


[PMID 22386478] Fibrinogen polymorphisms associated with sporadic cerebral hemorrhage in a Chinese population


[PMID 18513389OA-icon.png] New application of intelligent agents in sporadic amyotrophic lateral sclerosis identifies unexpected specific genetic background.


[PMID 18936436OA-icon.png] Prevalence in the United States of selected candidate gene variants: Third National Health and Nutrition Examination Survey, 1991-1994.


[PMID 19131662OA-icon.png] A meta-analysis of candidate gene polymorphisms and ischemic stroke in 6 study populations: association of lymphotoxin-alpha in nonhypertensive patients.


[PMID 19330901OA-icon.png] Association of 77 polymorphisms in 52 candidate genes with blood pressure progression and incident hypertension: the Women's Genome Health Study.


[PMID 19559392OA-icon.png] A candidate gene association study of 77 polymorphisms in migraine.


[PMID 19750100OA-icon.png] Modification of the interleukin-6 response to air pollution by interleukin-6 and fibrinogen polymorphisms.


[PMID 20031576OA-icon.png] Association of novel genetic Loci with circulating fibrinogen levels: a genome-wide association study in 6 population-based cohorts.


[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.


[PMID 20059469OA-icon.png] Interaction between fibrinogen and IL-6 genetic variants and associations with cardiovascular disease risk in the Cardiovascular Health Study.


[PMID 22267327] Fibrinogen and factor XIII A-subunit genotypes interactively influence C-reactive protein levels during inflammation.


[PMID 22388766OA-icon.png] A genetic instrument for Mendelian randomization of fibrinogen.


[PMID 23220916] Elevated fibrinogen levels are associated with risk of pulmonary embolism, but not with deep venous thrombosis.


[PMID 23274712OA-icon.png] Genetic polymorphisms and the risk of myocardial infarction in patients under 45 years of age.


[PMID 23944290] Association between two functional fibrinogen-related polymorphisms and ischemic stroke: a case-control study


[PMID 25862345] Genetic association between FXIII and β-fibrinogen genes and women with recurrent spontaneous abortion: a meta- analysis


[PMID 27277665] Genetic risk factors for restenosis after percutaneous coronary intervention in Kazakh population.