rs12566888
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs12566888(G;G) |
Make rs12566888(G;T) |
Make rs12566888(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 1 |
Position | 156899255 |
Gene | PEAR1 |
is a | snp |
is | mentioned by |
dbSNP | rs12566888 |
dbSNP (classic) | rs12566888 |
ClinGen | rs12566888 |
ebi | rs12566888 |
HLI | rs12566888 |
Exac | rs12566888 |
Gnomad | rs12566888 |
Varsome | rs12566888 |
LitVar | rs12566888 |
Map | rs12566888 |
PheGenI | rs12566888 |
Biobank | rs12566888 |
1000 genomes | rs12566888 |
hgdp | rs12566888 |
ensembl | rs12566888 |
geneview | rs12566888 |
scholar | rs12566888 |
rs12566888 | |
pharmgkb | rs12566888 |
gwascentral | rs12566888 |
openSNP | rs12566888 |
23andMe | rs12566888 |
SNPshot | rs12566888 |
SNPdbe | rs12566888 |
MSV3d | rs12566888 |
GWAS Ctlg | rs12566888 |
GMAF | 0.3232 |
Max Magnitude | 0 |
? | (G;G) (G;T) (T;T) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 20526338] |
Trait | Platelet aggregation |
Title | Genome-wide meta-analyses identifies seven loci associated with platelet aggregation in response
to agonists |
Risk Allele | A |
P-val | 5E-19 |
Odds Ratio | None None |
[PMID 25703520] Different Models of Inheritance in Selected Genes in Patients with Sticky Platelet Syndrome and Fetal Loss
[PMID 29867494] Variants of PEAR1 Are Associated With Outcome in Patients With ACS and Stable CAD Undergoing PCI.
[PMID 29865896] Association of Genetic Variability in Selected Genes in Patients With Deep Vein Thrombosis and Platelet Hyperaggregability.