rs3749147
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs3749147(C;C) |
| Make rs3749147(C;T) |
| Make rs3749147(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 2 |
| Position | 27629051 |
| Gene | CCDC121, GPN1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs3749147 |
| dbSNP (classic) | rs3749147 |
| ClinGen | rs3749147 |
| ebi | rs3749147 |
| HLI | rs3749147 |
| Exac | rs3749147 |
| Gnomad | rs3749147 |
| Varsome | rs3749147 |
| LitVar | rs3749147 |
| Map | rs3749147 |
| PheGenI | rs3749147 |
| Biobank | rs3749147 |
| 1000 genomes | rs3749147 |
| hgdp | rs3749147 |
| ensembl | rs3749147 |
| geneview | rs3749147 |
| scholar | rs3749147 |
| rs3749147 | |
| pharmgkb | rs3749147 |
| gwascentral | rs3749147 |
| openSNP | rs3749147 |
| 23andMe | rs3749147 |
| SNPshot | rs3749147 |
| SNPdbe | rs3749147 |
| MSV3d | rs3749147 |
| GWAS Ctlg | rs3749147 |
| GMAF | 0.23 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 21386085 ]
|
| Trait | |
| Title | A Bivariate Genome-Wide Approach to Metabolic Syndrome: STAMPEED Consortium |
| Risk Allele | C |
| P-val | 1E-9 |
| Odds Ratio | 0.1800 [0.12-0.24] unit decrease |
