rs7872802
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs7872802(A;A) |
Make rs7872802(A;G) |
Make rs7872802(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 9 |
Position | 129753451 |
Gene | PTGES |
is a | snp |
is | mentioned by |
dbSNP | rs7872802 |
dbSNP (classic) | rs7872802 |
ClinGen | rs7872802 |
ebi | rs7872802 |
HLI | rs7872802 |
Exac | rs7872802 |
Gnomad | rs7872802 |
Varsome | rs7872802 |
LitVar | rs7872802 |
Map | rs7872802 |
PheGenI | rs7872802 |
Biobank | rs7872802 |
1000 genomes | rs7872802 |
hgdp | rs7872802 |
ensembl | rs7872802 |
geneview | rs7872802 |
scholar | rs7872802 |
rs7872802 | |
pharmgkb | rs7872802 |
gwascentral | rs7872802 |
openSNP | rs7872802 |
23andMe | rs7872802 |
SNPshot | rs7872802 |
SNPdbe | rs7872802 |
MSV3d | rs7872802 |
GWAS Ctlg | rs7872802 |
GMAF | 0.2089 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 21816595] A Promoter polymorphism (rs17222919, -1316T/G) of ALOX5AP is associated with intracerebral hemorrhage in Korean population