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rs2519093

From SNPedia

Orientationplus
Stabilizedplus
Make rs2519093(C;C)
Make rs2519093(C;T)
Make rs2519093(T;T)
ReferenceGRCh38 38.1/141
Chromosome9
Position133266456
GeneABO
is asnp
is mentioned by
dbSNPrs2519093
ebirs2519093
HLIrs2519093
Exacrs2519093
Varsomers2519093
Maprs2519093
PheGenIrs2519093
hapmaprs2519093
1000 genomesrs2519093
hgdprs2519093
ensemblrs2519093
gopubmedrs2519093
geneviewrs2519093
scholarrs2519093
googlers2519093
pharmgkbrs2519093
gwascentralrs2519093
openSNPrs2519093
23andMers2519093
23andMe allrs2519093
SNP Nexus

SNPshotrs2519093
SNPdbers2519093
MSV3drs2519093
GWAS Ctlgrs2519093
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 22672568OA-icon.png]
Trait
Title A genome-wide association study of venous thromboembolism identifies risk variants in chromosomes 1q24.2 and 9q.
Risk Allele A
P-val 8E-16
Odds Ratio 1.6900 None

[PMID 21463476OA-icon.png] Genetic variation within the anticoagulant, procoagulant, fibrinolytic and innate immunity pathways as risk factors for venous thromboembolism.