rs467650
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs467650(C;C) |
Make rs467650(C;T) |
Make rs467650(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 5 |
Position | 98633749 |
is a | snp |
is | mentioned by |
dbSNP | rs467650 |
dbSNP (classic) | rs467650 |
ClinGen | rs467650 |
ebi | rs467650 |
HLI | rs467650 |
Exac | rs467650 |
Gnomad | rs467650 |
Varsome | rs467650 |
LitVar | rs467650 |
Map | rs467650 |
PheGenI | rs467650 |
Biobank | rs467650 |
1000 genomes | rs467650 |
hgdp | rs467650 |
ensembl | rs467650 |
geneview | rs467650 |
scholar | rs467650 |
rs467650 | |
pharmgkb | rs467650 |
gwascentral | rs467650 |
openSNP | rs467650 |
23andMe | rs467650 |
SNPshot | rs467650 |
SNPdbe | rs467650 |
MSV3d | rs467650 |
GWAS Ctlg | rs467650 |
GMAF | 0.3457 |
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 | 1E-8 |
Odds Ratio | 1.49 [NR] |