rs1866389
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs1866389(C;C) |
| Make rs1866389(C;G) |
| Make rs1866389(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 5 |
| Position | 80065442 |
| Gene | THBS4 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1866389 |
| dbSNP (classic) | rs1866389 |
| ClinGen | rs1866389 |
| ebi | rs1866389 |
| HLI | rs1866389 |
| Exac | rs1866389 |
| Gnomad | rs1866389 |
| Varsome | rs1866389 |
| LitVar | rs1866389 |
| Map | rs1866389 |
| PheGenI | rs1866389 |
| Biobank | rs1866389 |
| 1000 genomes | rs1866389 |
| hgdp | rs1866389 |
| ensembl | rs1866389 |
| geneview | rs1866389 |
| scholar | rs1866389 |
| rs1866389 | |
| pharmgkb | rs1866389 |
| gwascentral | rs1866389 |
| openSNP | rs1866389 |
| 23andMe | rs1866389 |
| SNPshot | rs1866389 |
| SNPdbe | rs1866389 |
| MSV3d | rs1866389 |
| GWAS Ctlg | rs1866389 |
| GMAF | 0.1359 |
| Max Magnitude | 0 |
| ? | (C;C) (C;G) (G;G) | 28 |
|---|---|---|
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| ||
[PMID 22011848] Thrombospondin-4 polymorphism (A387P) predicts cardiovascular risk in postinfarction patients with high HDL cholesterol and C-reactive protein levels
[PMID 18178577] Polymorphisms in thrombospondin genes and myocardial infarction: a case-control study and a meta-analysis of available evidence.
[PMID 18682748
] Analysis of 17,576 potentially functional SNPs in three case-control studies of myocardial infarction.
