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rs2036914

From SNPedia

Orientationplus
Stabilizedplus
Make rs2036914(C;C)
Make rs2036914(C;T)
Make rs2036914(T;T)
ReferenceGRCh38 38.1/141
Chromosome4
Position186271327
GeneF11
is asnp
is mentioned by
dbSNPrs2036914
ebirs2036914
HLIrs2036914
Exacrs2036914
Varsomers2036914
Maprs2036914
PheGenIrs2036914
hapmaprs2036914
1000 genomesrs2036914
hgdprs2036914
ensemblrs2036914
gopubmedrs2036914
geneviewrs2036914
scholarrs2036914
googlers2036914
pharmgkbrs2036914
gwascentralrs2036914
openSNPrs2036914
23andMers2036914
23andMe allrs2036914
SNP Nexus

SNPshotrs2036914
SNPdbers2036914
MSV3drs2036914
GWAS Ctlgrs2036914
GMAF0.3678
Max Magnitude
? (C;C) (C;T) (T;T) 28

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


[PMID 21232005OA-icon.png] New gene variants associated with venous thrombosis: a replication study in White and Black Americans.


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


[PMID 25210051] Genetic Variations Associated with Recurrent Venous Thrombosis