rs1501908
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs1501908(C;C) |
| Make rs1501908(C;G) |
| Make rs1501908(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 5 |
| Position | 156971158 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1501908 |
| dbSNP (classic) | rs1501908 |
| ClinGen | rs1501908 |
| ebi | rs1501908 |
| HLI | rs1501908 |
| Exac | rs1501908 |
| Gnomad | rs1501908 |
| Varsome | rs1501908 |
| LitVar | rs1501908 |
| Map | rs1501908 |
| PheGenI | rs1501908 |
| Biobank | rs1501908 |
| 1000 genomes | rs1501908 |
| hgdp | rs1501908 |
| ensembl | rs1501908 |
| geneview | rs1501908 |
| scholar | rs1501908 |
| rs1501908 | |
| pharmgkb | rs1501908 |
| gwascentral | rs1501908 |
| openSNP | rs1501908 |
| 23andMe | rs1501908 |
| SNPshot | rs1501908 |
| SNPdbe | rs1501908 |
| MSV3d | rs1501908 |
| GWAS Ctlg | rs1501908 |
| GMAF | 0.3843 |
| Max Magnitude | 0 |
| ? | (C;C) (C;G) (G;G) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 19060906 ]
|
| Trait | LDL cholesterol |
| Title | Common variants at 30 loci contribute to polygenic dyslipidemia |
| Risk Allele | G |
| P-val | 1E-11 |
| Odds Ratio | 0.07 [0.03-0.11] SD decrease |
[PMID 19951432] Analysis of recently identified dyslipidemia alleles reveals two loci that contribute to risk for carotid artery disease.
