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rs7714670

From SNPedia

Orientationplus
Stabilizedplus
Make rs7714670(C;C)
Make rs7714670(C;T)
Make rs7714670(T;T)
ReferenceGRCh38 38.1/141
Chromosome5
Position73776529
GeneCCDC39
is asnp
is mentioned by
dbSNPrs7714670
ebirs7714670
HLIrs7714670
Exacrs7714670
Varsomers7714670
Maprs7714670
PheGenIrs7714670
hapmaprs7714670
1000 genomesrs7714670
hgdprs7714670
ensemblrs7714670
gopubmedrs7714670
geneviewrs7714670
scholarrs7714670
googlers7714670
pharmgkbrs7714670
gwascentralrs7714670
openSNPrs7714670
23andMers7714670
23andMe allrs7714670
SNP Nexus

SNPshotrs7714670
SNPdbers7714670
MSV3drs7714670
GWAS Ctlgrs7714670
GMAF0.377
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 A
P-val 2E-9
Odds Ratio 1.52 [NR]