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rs493014

From SNPedia

Orientationplus
Stabilizedplus
Make rs493014(G;G)
Make rs493014(G;T)
Make rs493014(T;T)
ReferenceGRCh38 38.1/141
Chromosome9
Position133320327
is asnp
is mentioned by
dbSNPrs493014
ebirs493014
HLIrs493014
Exacrs493014
Varsomers493014
Maprs493014
PheGenIrs493014
hapmaprs493014
1000 genomesrs493014
hgdprs493014
ensemblrs493014
gopubmedrs493014
geneviewrs493014
scholarrs493014
googlers493014
pharmgkbrs493014
gwascentralrs493014
openSNPrs493014
23andMers493014
23andMe allrs493014
SNP Nexus

SNPshotrs493014
SNPdbers493014
MSV3drs493014
GWAS Ctlgrs493014
GMAF0.3095
Max Magnitude
? (G;G) (G;T) (T;T) 28
GWAS snp
PMID [PMID 23509962OA-icon.png]
Trait Venous thromboembolism (gene x gene interaction)
Title A genome-wide search for common SNP x SNP interactions on the risk of venous thrombosis.
Risk Allele A
P-val 6E-11
Odds Ratio 1.64 [NR]