rs1364505
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs1364505(A;A) |
Make rs1364505(A;G) |
Make rs1364505(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 7 |
Position | 132345252 |
Gene | PLXNA4 |
is a | snp |
is | mentioned by |
dbSNP | rs1364505 |
dbSNP (classic) | rs1364505 |
ClinGen | rs1364505 |
ebi | rs1364505 |
HLI | rs1364505 |
Exac | rs1364505 |
Gnomad | rs1364505 |
Varsome | rs1364505 |
LitVar | rs1364505 |
Map | rs1364505 |
PheGenI | rs1364505 |
Biobank | rs1364505 |
1000 genomes | rs1364505 |
hgdp | rs1364505 |
ensembl | rs1364505 |
geneview | rs1364505 |
scholar | rs1364505 |
rs1364505 | |
pharmgkb | rs1364505 |
gwascentral | rs1364505 |
openSNP | rs1364505 |
23andMe | rs1364505 |
SNPshot | rs1364505 |
SNPdbe | rs1364505 |
MSV3d | rs1364505 |
GWAS Ctlg | rs1364505 |
GMAF | 0.3026 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 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 | A |
P-val | 2E-9 |
Odds Ratio | 1.80 [NR] |