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rs318497

From SNPedia

Orientationplus
Stabilizedplus
Make rs318497(A;A)
Make rs318497(A;G)
Make rs318497(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position2912043
is asnp
is mentioned by
dbSNPrs318497
ebirs318497
HLIrs318497
Exacrs318497
Varsomers318497
Maprs318497
PheGenIrs318497
hapmaprs318497
1000 genomesrs318497
hgdprs318497
ensemblrs318497
gopubmedrs318497
geneviewrs318497
scholarrs318497
googlers318497
pharmgkbrs318497
gwascentralrs318497
openSNPrs318497
23andMers318497
23andMe allrs318497
SNP Nexus

SNPshotrs318497
SNPdbers318497
MSV3drs318497
GWAS Ctlgrs318497
GMAF0.4793
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
P-val 5E-9
Odds Ratio 2.33 [NR]