rs10516089
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs10516089(C;C) |
Make rs10516089(C;T) |
Make rs10516089(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 5 |
Position | 171724227 |
Gene | LOC105377724 |
is a | snp |
is | mentioned by |
dbSNP | rs10516089 |
dbSNP (classic) | rs10516089 |
ClinGen | rs10516089 |
ebi | rs10516089 |
HLI | rs10516089 |
Exac | rs10516089 |
Gnomad | rs10516089 |
Varsome | rs10516089 |
LitVar | rs10516089 |
Map | rs10516089 |
PheGenI | rs10516089 |
Biobank | rs10516089 |
1000 genomes | rs10516089 |
hgdp | rs10516089 |
ensembl | rs10516089 |
geneview | rs10516089 |
scholar | rs10516089 |
rs10516089 | |
pharmgkb | rs10516089 |
gwascentral | rs10516089 |
openSNP | rs10516089 |
23andMe | rs10516089 |
SNPshot | rs10516089 |
SNPdbe | rs10516089 |
MSV3d | rs10516089 |
GWAS Ctlg | rs10516089 |
GMAF | 0.3646 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 23509962] |
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 | 4E-9 |
Odds Ratio | 1.59 [NR] |