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rs2771051

From SNPedia

Orientationplus
Stabilizedplus
Make rs2771051(G;G)
Make rs2771051(G;T)
Make rs2771051(T;T)
ReferenceGRCh38 38.1/141
Chromosome9
Position117525430
is asnp
is mentioned by
dbSNPrs2771051
ebirs2771051
HLIrs2771051
Exacrs2771051
Varsomers2771051
Maprs2771051
PheGenIrs2771051
hapmaprs2771051
1000 genomesrs2771051
hgdprs2771051
ensemblrs2771051
gopubmedrs2771051
geneviewrs2771051
scholarrs2771051
googlers2771051
pharmgkbrs2771051
gwascentralrs2771051
openSNPrs2771051
23andMers2771051
23andMe allrs2771051
SNP Nexus

SNPshotrs2771051
SNPdbers2771051
MSV3drs2771051
GWAS Ctlgrs2771051
GMAF0.4945
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
P-val 4E-9
Odds Ratio 1.49 [NR]