rs3733860
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs3733860(A;A) |
Make rs3733860(A;C) |
Make rs3733860(C;C) |
Reference | GRCh38 38.1/141 |
Chromosome | 5 |
Position | 76326989 |
Gene | SV2C |
is a | snp |
is | mentioned by |
dbSNP | rs3733860 |
dbSNP (classic) | rs3733860 |
ClinGen | rs3733860 |
ebi | rs3733860 |
HLI | rs3733860 |
Exac | rs3733860 |
Gnomad | rs3733860 |
Varsome | rs3733860 |
LitVar | rs3733860 |
Map | rs3733860 |
PheGenI | rs3733860 |
Biobank | rs3733860 |
1000 genomes | rs3733860 |
hgdp | rs3733860 |
ensembl | rs3733860 |
geneview | rs3733860 |
scholar | rs3733860 |
rs3733860 | |
pharmgkb | rs3733860 |
gwascentral | rs3733860 |
openSNP | rs3733860 |
23andMe | rs3733860 |
SNPshot | rs3733860 |
SNPdbe | rs3733860 |
MSV3d | rs3733860 |
GWAS Ctlg | rs3733860 |
GMAF | 0.1896 |
Max Magnitude | 0 |
? | (A;A) (A;C) (C;C) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 23650146] |
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] |