rs12408810
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs12408810(C;C) |
| Make rs12408810(C;T) |
| Make rs12408810(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 1 |
| Position | 106098321 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs12408810 |
| dbSNP (classic) | rs12408810 |
| ClinGen | rs12408810 |
| ebi | rs12408810 |
| HLI | rs12408810 |
| Exac | rs12408810 |
| Gnomad | rs12408810 |
| Varsome | rs12408810 |
| LitVar | rs12408810 |
| Map | rs12408810 |
| PheGenI | rs12408810 |
| Biobank | rs12408810 |
| 1000 genomes | rs12408810 |
| hgdp | rs12408810 |
| ensembl | rs12408810 |
| geneview | rs12408810 |
| scholar | rs12408810 |
| rs12408810 | |
| pharmgkb | rs12408810 |
| gwascentral | rs12408810 |
| openSNP | rs12408810 |
| 23andMe | rs12408810 |
| SNPshot | rs12408810 |
| SNPdbe | rs12408810 |
| MSV3d | rs12408810 |
| GWAS Ctlg | rs12408810 |
| GMAF | 0.2599 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 23563609 ]
|
| Trait | Obesity (early onset extreme) |
| Title | Genome-wide SNP and CNV analysis identifies common and low-frequency variants associated with severe early-onset obesity. |
| Risk Allele | C |
| P-val | 9E-6 |
| Odds Ratio | 1.25 [1.13-1.38] |
