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rs2066865

From SNPedia

Orientationminus
Stabilizedminus
Make rs2066865(C;C)
Make rs2066865(C;T)
Make rs2066865(T;T)
ReferenceGRCh38 38.1/141
Chromosome4
Position154604124
GeneFGG
is asnp
is mentioned by
dbSNPrs2066865
ebirs2066865
HLIrs2066865
Exacrs2066865
Varsomers2066865
Maprs2066865
PheGenIrs2066865
hapmaprs2066865
1000 genomesrs2066865
hgdprs2066865
ensemblrs2066865
gopubmedrs2066865
geneviewrs2066865
scholarrs2066865
googlers2066865
pharmgkbrs2066865
gwascentralrs2066865
openSNPrs2066865
23andMers2066865
23andMe allrs2066865
SNP Nexus

SNPshotrs2066865
SNPdbers2066865
MSV3drs2066865
GWAS Ctlgrs2066865
GMAF0.3186
Max Magnitude
? (C;C) (C;T) (T;T) 28
[PMID 20167083OA-icon.png] Fibrinogen beta variants confer protection against coronary artery disease in a Greek case-control study


[PMID 20709368] The fibrinogen gamma 10034C>T polymorphism is not associated with Peripheral Arterial Disease


[PMID 22707612OA-icon.png] Genetic Risk Factors for Thrombosis in Systemic Lupus Erythematosus

[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 23150947] Single nucleotide polymorphisms and the risk of venous thrombosis: results from a Danish case-cohort study


[PMID 25091233] Association of F11 polymorphism rs2289252 with deep vein thrombosis and related phenotypes in population of Latvia


[PMID 25210051] Genetic Variations Associated with Recurrent Venous Thrombosis