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rs7648704

From SNPedia

Orientationplus
Stabilizedplus
Make rs7648704(G;G)
Make rs7648704(G;T)
Make rs7648704(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position32900360
is asnp
is mentioned by
dbSNPrs7648704
dbSNP (classic)rs7648704
ClinGenrs7648704
ebirs7648704
HLIrs7648704
Exacrs7648704
Gnomadrs7648704
Varsomers7648704
LitVarrs7648704
Maprs7648704
PheGenIrs7648704
Biobankrs7648704
1000 genomesrs7648704
hgdprs7648704
ensemblrs7648704
geneviewrs7648704
scholarrs7648704
googlers7648704
pharmgkbrs7648704
gwascentralrs7648704
openSNPrs7648704
23andMers7648704
SNPshotrs7648704
SNPdbers7648704
MSV3drs7648704
GWAS Ctlgrs7648704
GMAF0.354
Max Magnitude0
? (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 T
P-val 1E-9
Odds Ratio 1.56 [NR]