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rs467650

From SNPedia

Orientationplus
Stabilizedplus
Make rs467650(C;C)
Make rs467650(C;T)
Make rs467650(T;T)
ReferenceGRCh38 38.1/141
Chromosome5
Position98633749
is asnp
is mentioned by
dbSNPrs467650
ebirs467650
HLIrs467650
Exacrs467650
Varsomers467650
Maprs467650
PheGenIrs467650
hapmaprs467650
1000 genomesrs467650
hgdprs467650
ensemblrs467650
gopubmedrs467650
geneviewrs467650
scholarrs467650
googlers467650
pharmgkbrs467650
gwascentralrs467650
openSNPrs467650
23andMers467650
23andMe allrs467650
SNP Nexus

SNPshotrs467650
SNPdbers467650
MSV3drs467650
GWAS Ctlgrs467650
GMAF0.3457
Max Magnitude
? (C;C) (C;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 1E-8
Odds Ratio 1.49 [NR]