rs2660899
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs2660899(G;G) |
| Make rs2660899(G;T) |
| Make rs2660899(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 12 |
| Position | 96036642 |
| Gene | LTA4H |
| is a | snp |
| is | mentioned by |
| dbSNP | rs2660899 |
| dbSNP (classic) | rs2660899 |
| ClinGen | rs2660899 |
| ebi | rs2660899 |
| HLI | rs2660899 |
| Exac | rs2660899 |
| Gnomad | rs2660899 |
| Varsome | rs2660899 |
| LitVar | rs2660899 |
| Map | rs2660899 |
| PheGenI | rs2660899 |
| Biobank | rs2660899 |
| 1000 genomes | rs2660899 |
| hgdp | rs2660899 |
| ensembl | rs2660899 |
| geneview | rs2660899 |
| scholar | rs2660899 |
| rs2660899 | |
| pharmgkb | rs2660899 |
| gwascentral | rs2660899 |
| openSNP | rs2660899 |
| 23andMe | rs2660899 |
| SNPshot | rs2660899 |
| SNPdbe | rs2660899 |
| MSV3d | rs2660899 |
| GWAS Ctlg | rs2660899 |
| GMAF | 0.2691 |
| Max Magnitude | 0 |
| ? | (G;G) (G;T) (T;T) | 28 |
|---|---|---|
|
| ||
Despite earlier reports of an association, no risk for myocardial infarction was seen for rs2660899 variants in a study of 1,211 German patients. [PMID 18318662]
