rs4129767
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs4129767(C;C) |
| Make rs4129767(C;T) |
| Make rs4129767(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 17 |
| Position | 78407903 |
| Gene | PGS1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs4129767 |
| dbSNP (classic) | rs4129767 |
| ClinGen | rs4129767 |
| ebi | rs4129767 |
| HLI | rs4129767 |
| Exac | rs4129767 |
| Gnomad | rs4129767 |
| Varsome | rs4129767 |
| LitVar | rs4129767 |
| Map | rs4129767 |
| PheGenI | rs4129767 |
| Biobank | rs4129767 |
| 1000 genomes | rs4129767 |
| hgdp | rs4129767 |
| ensembl | rs4129767 |
| geneview | rs4129767 |
| scholar | rs4129767 |
| rs4129767 | |
| pharmgkb | rs4129767 |
| gwascentral | rs4129767 |
| openSNP | rs4129767 |
| 23andMe | rs4129767 |
| SNPshot | rs4129767 |
| SNPdbe | rs4129767 |
| MSV3d | rs4129767 |
| GWAS Ctlg | rs4129767 |
| GMAF | 0.4449 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 20686565 ]
|
| Trait | |
| Title | Biological, clinical and population relevance of 95 loci for blood lipids. |
| Risk Allele | G |
| P-val | 5E-9 |
| Odds Ratio | 0.4000 None |
| GWAS snp | |
|---|---|
| PMID | [PMID 24097068]
|
| Trait | HDL cholesterol |
| Title | Discovery and refinement of loci associated with lipid levels. |
| Risk Allele | G |
| P-val | 2E-11 |
| Odds Ratio | .02 [NR] unit decrease |
