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rs3733860

From SNPedia

Orientationplus
Stabilizedplus
Make rs3733860(A;A)
Make rs3733860(A;C)
Make rs3733860(C;C)
ReferenceGRCh38 38.1/141
Chromosome5
Position76326989
GeneSV2C
is asnp
is mentioned by
dbSNPrs3733860
ebirs3733860
HLIrs3733860
Exacrs3733860
Varsomers3733860
Maprs3733860
PheGenIrs3733860
hapmaprs3733860
1000 genomesrs3733860
hgdprs3733860
ensemblrs3733860
gopubmedrs3733860
geneviewrs3733860
scholarrs3733860
googlers3733860
pharmgkbrs3733860
gwascentralrs3733860
openSNPrs3733860
23andMers3733860
23andMe allrs3733860
SNP Nexus

SNPshotrs3733860
SNPdbers3733860
MSV3drs3733860
GWAS Ctlgrs3733860
GMAF0.1896
Max Magnitude
? (A;A) (A;C) (C;C) 28
GWAS snp
PMID [PMID 23650146OA-icon.png]
Trait Venous thromboembolism
Title A genome-wide association study for venous thromboembolism: the extended cohorts for heart and aging research in genomic epidemiology (CHARGE) consortium.
Risk Allele A
P-val 8E-6
Odds Ratio 1.19 [1.10-1.29]