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rs2028385

From SNPedia

Orientationplus
Stabilizedplus
Make rs2028385(A;A)
Make rs2028385(A;G)
Make rs2028385(G;G)
ReferenceGRCh38 38.1/141
Chromosome12
Position96423644
is asnp
is mentioned by
dbSNPrs2028385
ebirs2028385
HLIrs2028385
Exacrs2028385
Varsomers2028385
Maprs2028385
PheGenIrs2028385
hapmaprs2028385
1000 genomesrs2028385
hgdprs2028385
ensemblrs2028385
gopubmedrs2028385
geneviewrs2028385
scholarrs2028385
googlers2028385
pharmgkbrs2028385
gwascentralrs2028385
openSNPrs2028385
23andMers2028385
23andMe allrs2028385
SNP Nexus

SNPshotrs2028385
SNPdbers2028385
MSV3drs2028385
GWAS Ctlgrs2028385
GMAF0.2296
Max Magnitude
? (A;A) (A;G) (G;G) 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 C
P-val 9E-9
Odds Ratio 1.69 [NR]