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rs2289252

From SNPedia

Orientationplus
Stabilizedplus
Make rs2289252(C;C)
Make rs2289252(C;T)
Make rs2289252(T;T)
ReferenceGRCh38 38.1/141
Chromosome4
Position186286227
GeneF11, PRAMEF4
is asnp
is mentioned by
dbSNPrs2289252
ebirs2289252
HLIrs2289252
Exacrs2289252
Varsomers2289252
Maprs2289252
PheGenIrs2289252
hapmaprs2289252
1000 genomesrs2289252
hgdprs2289252
ensemblrs2289252
gopubmedrs2289252
geneviewrs2289252
scholarrs2289252
googlers2289252
pharmgkbrs2289252
gwascentralrs2289252
openSNPrs2289252
23andMers2289252
23andMe allrs2289252
SNP Nexus

SNPshotrs2289252
SNPdbers2289252
MSV3drs2289252
GWAS Ctlgrs2289252
GMAF0.3343
Max Magnitude
? (C;C) (C;T) (T;T) 28

[PMID 19583818] Genetic variants associated with deep vein thrombosis: the F11 locus


[PMID 22633531] The F11 rs2289252 polymorphism is associated with FXI activity levels and APTT ratio in women with thrombosis


[PMID 19552680OA-icon.png] Common hemostasis and inflammation gene variants and venous thrombosis in older adults from the Cardiovascular Health Study.


[PMID 20031567OA-icon.png] An evaluation of candidate genes of inflammation and thrombosis in relation to the risk of venous thromboembolism: The Women's Genome Health Study.


[PMID 20352152] Association of common genetic variations and idiopathic venous thromboembolism. Results from EDITh, a hospital-based case-control study.


[PMID 22533697] Candidate gene polymorphisms and the risk for pregnancy-related venous thrombosis.

GWAS snp
PMID [PMID 22703881OA-icon.png]
Trait
Title Genetic Associations for Activated Partial Thromboplastin Time and Prothrombin Time, their Gene Expression Profiles, and Risk of Coronary Artery Disease.
Risk Allele C
P-val 6E-43
Odds Ratio 0.4830 None


[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