rs5628
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in complete genomics |
Make rs5628(C;T) |
Make rs5628(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 20 |
Position | 49524145 |
Gene | PTGIS |
is a | snp |
is | mentioned by |
dbSNP | rs5628 |
dbSNP (classic) | rs5628 |
ClinGen | rs5628 |
ebi | rs5628 |
HLI | rs5628 |
Exac | rs5628 |
Gnomad | rs5628 |
Varsome | rs5628 |
LitVar | rs5628 |
Map | rs5628 |
PheGenI | rs5628 |
Biobank | rs5628 |
1000 genomes | rs5628 |
hgdp | rs5628 |
ensembl | rs5628 |
geneview | rs5628 |
scholar | rs5628 |
rs5628 | |
pharmgkb | rs5628 |
gwascentral | rs5628 |
openSNP | rs5628 |
23andMe | rs5628 |
SNPshot | rs5628 |
SNPdbe | rs5628 |
MSV3d | rs5628 |
GWAS Ctlg | rs5628 |
GMAF | 0.1047 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
[PMID 21816595] A Promoter polymorphism (rs17222919, -1316T/G) of ALOX5AP is associated with intracerebral hemorrhage in Korean population
[PMID 19046748] Variation in eicosanoid genes, non-fatal myocardial infarction and ischemic stroke.