rs4360791
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs4360791(A;A) |
Make rs4360791(A;G) |
Make rs4360791(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 13 |
Position | 30743883 |
Gene | ALOX5AP |
is a | snp |
is | mentioned by |
dbSNP | rs4360791 |
dbSNP (classic) | rs4360791 |
ClinGen | rs4360791 |
ebi | rs4360791 |
HLI | rs4360791 |
Exac | rs4360791 |
Gnomad | rs4360791 |
Varsome | rs4360791 |
LitVar | rs4360791 |
Map | rs4360791 |
PheGenI | rs4360791 |
Biobank | rs4360791 |
1000 genomes | rs4360791 |
hgdp | rs4360791 |
ensembl | rs4360791 |
geneview | rs4360791 |
scholar | rs4360791 |
rs4360791 | |
pharmgkb | rs4360791 |
gwascentral | rs4360791 |
openSNP | rs4360791 |
23andMe | rs4360791 |
SNPshot | rs4360791 |
SNPdbe | rs4360791 |
MSV3d | rs4360791 |
GWAS Ctlg | rs4360791 |
GMAF | 0.4403 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 22051033] ALOX5AP genetic variants and risk of atherothrombotic stroke in the Taiwanese population