rs4660293
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs4660293(A;A) |
| Make rs4660293(A;G) |
| Make rs4660293(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 1 |
| Position | 39562508 |
| Gene | PABPC4 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs4660293 |
| dbSNP (classic) | rs4660293 |
| ClinGen | rs4660293 |
| ebi | rs4660293 |
| HLI | rs4660293 |
| Exac | rs4660293 |
| Gnomad | rs4660293 |
| Varsome | rs4660293 |
| LitVar | rs4660293 |
| Map | rs4660293 |
| PheGenI | rs4660293 |
| Biobank | rs4660293 |
| 1000 genomes | rs4660293 |
| hgdp | rs4660293 |
| ensembl | rs4660293 |
| geneview | rs4660293 |
| scholar | rs4660293 |
| rs4660293 | |
| pharmgkb | rs4660293 |
| gwascentral | rs4660293 |
| openSNP | rs4660293 |
| 23andMe | rs4660293 |
| SNPshot | rs4660293 |
| SNPdbe | rs4660293 |
| MSV3d | rs4660293 |
| GWAS Ctlg | rs4660293 |
| GMAF | 0.1423 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 20686565 ]
|
| Trait | |
| Title | Biological, clinical and population relevance of 95 loci for blood lipids. |
| Risk Allele | G |
| P-val | 4E-10 |
| Odds Ratio | 0.4800 None |
[PMID 23160641] Exome sequencing-driven discovery of coding polymorphisms associated with common metabolic phenotypes.
| GWAS snp | |
|---|---|
| PMID | [PMID 24097068]
|
| Trait | HDL cholesterol |
| Title | Discovery and refinement of loci associated with lipid levels. |
| Risk Allele | G |
| P-val | 3E-18 |
| Odds Ratio | .04 [NR] unit decrease |
[PMID 26005159] Gender-specific association between the cytoplasmic poly(A) binding protein 4 rs4660293 single nucleotide polymorphism and serum lipid levels
