rs4253399
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs4253399(G;G) |
Make rs4253399(G;T) |
Make rs4253399(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 4 |
Position | 186266940 |
Gene | F11 |
is a | snp |
is | mentioned by |
dbSNP | rs4253399 |
dbSNP (classic) | rs4253399 |
ClinGen | rs4253399 |
ebi | rs4253399 |
HLI | rs4253399 |
Exac | rs4253399 |
Gnomad | rs4253399 |
Varsome | rs4253399 |
LitVar | rs4253399 |
Map | rs4253399 |
PheGenI | rs4253399 |
Biobank | rs4253399 |
1000 genomes | rs4253399 |
hgdp | rs4253399 |
ensembl | rs4253399 |
geneview | rs4253399 |
scholar | rs4253399 |
rs4253399 | |
pharmgkb | rs4253399 |
gwascentral | rs4253399 |
openSNP | rs4253399 |
23andMe | rs4253399 |
SNPshot | rs4253399 |
SNPdbe | rs4253399 |
MSV3d | rs4253399 |
GWAS Ctlg | rs4253399 |
GMAF | 0.2833 |
Max Magnitude | 0 |
? | (G;G) (G;T) (T;T) | 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 | G |
P-val | 3E-14 |
Odds Ratio | 1.24 [1.17-1.31] |