rs4635554
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs4635554(G;G) |
| Make rs4635554(G;T) |
| Make rs4635554(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 2 |
| Position | 21166787 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs4635554 |
| dbSNP (classic) | rs4635554 |
| ClinGen | rs4635554 |
| ebi | rs4635554 |
| HLI | rs4635554 |
| Exac | rs4635554 |
| Gnomad | rs4635554 |
| Varsome | rs4635554 |
| LitVar | rs4635554 |
| Map | rs4635554 |
| PheGenI | rs4635554 |
| Biobank | rs4635554 |
| 1000 genomes | rs4635554 |
| hgdp | rs4635554 |
| ensembl | rs4635554 |
| geneview | rs4635554 |
| scholar | rs4635554 |
| rs4635554 | |
| pharmgkb | rs4635554 |
| gwascentral | rs4635554 |
| openSNP | rs4635554 |
| 23andMe | rs4635554 |
| SNPshot | rs4635554 |
| SNPdbe | rs4635554 |
| MSV3d | rs4635554 |
| GWAS Ctlg | rs4635554 |
| GMAF | 0.393 |
| Max Magnitude | 0 |
| ? | (G;G) (G;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 20657596 ]
|
| Trait | Hypertriglyceridemia |
| Title | Excess of rare variants in genes identified by genome-wide association study of hypertriglyceridemia |
| Risk Allele | G |
| P-val | 2E-7 |
| Odds Ratio | 1.67 [1.38-2.02] |
