rs2097055
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs2097055(C;C) |
| Make rs2097055(C;T) |
| Make rs2097055(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 18 |
| Position | 49569117 |
| Gene | LIPG |
| is a | snp |
| is | mentioned by |
| dbSNP | rs2097055 |
| dbSNP (classic) | rs2097055 |
| ClinGen | rs2097055 |
| ebi | rs2097055 |
| HLI | rs2097055 |
| Exac | rs2097055 |
| Gnomad | rs2097055 |
| Varsome | rs2097055 |
| LitVar | rs2097055 |
| Map | rs2097055 |
| PheGenI | rs2097055 |
| Biobank | rs2097055 |
| 1000 genomes | rs2097055 |
| hgdp | rs2097055 |
| ensembl | rs2097055 |
| geneview | rs2097055 |
| scholar | rs2097055 |
| rs2097055 | |
| pharmgkb | rs2097055 |
| gwascentral | rs2097055 |
| openSNP | rs2097055 |
| 23andMe | rs2097055 |
| SNPshot | rs2097055 |
| SNPdbe | rs2097055 |
| MSV3d | rs2097055 |
| GWAS Ctlg | rs2097055 |
| GMAF | 0.4954 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 20466371] Lack of association between common genetic variation in endothelial lipase (LIPG) and the risk for CAD and DVT
