rs6102059
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs6102059(C;C) |
| Make rs6102059(C;T) |
| Make rs6102059(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 20 |
| Position | 40600144 |
| Gene | LOC102724968 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs6102059 |
| dbSNP (classic) | rs6102059 |
| ClinGen | rs6102059 |
| ebi | rs6102059 |
| HLI | rs6102059 |
| Exac | rs6102059 |
| Gnomad | rs6102059 |
| Varsome | rs6102059 |
| LitVar | rs6102059 |
| Map | rs6102059 |
| PheGenI | rs6102059 |
| Biobank | rs6102059 |
| 1000 genomes | rs6102059 |
| hgdp | rs6102059 |
| ensembl | rs6102059 |
| geneview | rs6102059 |
| scholar | rs6102059 |
| rs6102059 | |
| pharmgkb | rs6102059 |
| gwascentral | rs6102059 |
| openSNP | rs6102059 |
| 23andMe | rs6102059 |
| SNPshot | rs6102059 |
| SNPdbe | rs6102059 |
| MSV3d | rs6102059 |
| GWAS Ctlg | rs6102059 |
| GMAF | 0.3875 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 19060906 ]
|
| Trait | LDL cholesterol |
| Title | Common variants at 30 loci contribute to polygenic dyslipidemia |
| Risk Allele | T |
| P-val | 4E-9 |
| Odds Ratio | 0.06 [0.03-0.10] SD decrease |
[PMID 21738485] Genetic determinants of lipid traits in diverse populations from the population architecture using genomics and epidemiology (PAGE) study
[PMID 19951432] Analysis of recently identified dyslipidemia alleles reveals two loci that contribute to risk for carotid artery disease.
