rs1260333
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs1260333(C;C) |
| Make rs1260333(C;T) |
| Make rs1260333(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 2 |
| Position | 27525757 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1260333 |
| dbSNP (classic) | rs1260333 |
| ClinGen | rs1260333 |
| ebi | rs1260333 |
| HLI | rs1260333 |
| Exac | rs1260333 |
| Gnomad | rs1260333 |
| Varsome | rs1260333 |
| LitVar | rs1260333 |
| Map | rs1260333 |
| PheGenI | rs1260333 |
| Biobank | rs1260333 |
| 1000 genomes | rs1260333 |
| hgdp | rs1260333 |
| ensembl | rs1260333 |
| geneview | rs1260333 |
| scholar | rs1260333 |
| rs1260333 | |
| pharmgkb | rs1260333 |
| gwascentral | rs1260333 |
| openSNP | rs1260333 |
| 23andMe | rs1260333 |
| SNPshot | rs1260333 |
| SNPdbe | rs1260333 |
| MSV3d | rs1260333 |
| GWAS Ctlg | rs1260333 |
| GMAF | 0.4513 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 20864672 ]
|
| Trait | |
| Title | Genetic Variants Influencing Circulating Lipid Levels and Risk of Coronary Artery Disease |
| Risk Allele | C |
| P-val | 2E-19 |
| Odds Ratio | 0.05 [0.04-0.06] unit decrease |
[PMID 18439548] Loci related to metabolic-syndrome pathways including LEPR,HNF1A, IL6R, and GCKR associate with plasma C-reactive protein: the Women's Genome Health Study.
[PMID 18439552] Polymorphisms of the HNF1A gene encoding hepatocyte nuclear factor-1 alpha are associated with C-reactive protein.
[PMID 23832694] Common genetic variants associated with lipid profiles in a Chinese pediatric population.
[PMID 31910446] Genome-wide association study of metabolic syndrome in Korean populations.
