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rs10476160

From SNPedia

Orientationplus
Stabilizedplus
Make rs10476160(A;A)
Make rs10476160(A;G)
Make rs10476160(G;G)
ReferenceGRCh38 38.1/141
Chromosome5
Position175547573
is asnp
is mentioned by
dbSNPrs10476160
dbSNP (classic)rs10476160
ClinGenrs10476160
ebirs10476160
HLIrs10476160
Exacrs10476160
Gnomadrs10476160
Varsomers10476160
LitVarrs10476160
Maprs10476160
PheGenIrs10476160
Biobankrs10476160
1000 genomesrs10476160
hgdprs10476160
ensemblrs10476160
geneviewrs10476160
scholarrs10476160
googlers10476160
pharmgkbrs10476160
gwascentralrs10476160
openSNPrs10476160
23andMers10476160
23andMe allrs10476160
SNPshotrs10476160
SNPdbers10476160
MSV3drs10476160
GWAS Ctlgrs10476160
GMAF0.3173
Max Magnitude0
? (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 9E-9
Odds Ratio 1.61 [NR]