rs17114036
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (A;A) | 0 | common/normal |
| Make rs17114036(A;G) |
| Make rs17114036(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 1 |
| Position | 56497149 |
| Gene | PLPP3 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs17114036 |
| dbSNP (classic) | rs17114036 |
| ClinGen | rs17114036 |
| ebi | rs17114036 |
| HLI | rs17114036 |
| Exac | rs17114036 |
| Gnomad | rs17114036 |
| Varsome | rs17114036 |
| LitVar | rs17114036 |
| Map | rs17114036 |
| PheGenI | rs17114036 |
| Biobank | rs17114036 |
| 1000 genomes | rs17114036 |
| hgdp | rs17114036 |
| ensembl | rs17114036 |
| geneview | rs17114036 |
| scholar | rs17114036 |
| rs17114036 | |
| pharmgkb | rs17114036 |
| gwascentral | rs17114036 |
| openSNP | rs17114036 |
| 23andMe | rs17114036 |
| SNPshot | rs17114036 |
| SNPdbe | rs17114036 |
| MSV3d | rs17114036 |
| GWAS Ctlg | rs17114036 |
| GMAF | 0.08953 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 24262325 ]
|
| Trait | Coronary artery disease |
| Title | Shared genetic susceptibility to ischemic stroke and coronary artery disease: a genome-wide analysis of common variants. |
| Risk Allele | G |
| P-val | 1E-8 |
| Odds Ratio | 1.15 [1.1-1.22] |
| GWAS snp | |
|---|---|
| PMID | [PMID 21378990]
|
| Trait | Coronary heart disease |
| Title | Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease |
| Risk Allele | A |
| P-val | 4E-19 |
| Odds Ratio | 1.1700 [1.13-1.22] |
[PMID 23202125] Large-scale association analysis identifies new risk loci for coronary artery disease.
[PMID 23161703] Influence of 23 coronary artery disease variants on recurrent myocardial infarction or cardiac death: the GRACE Genetics Study.
