rs2275848
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs2275848(G;G) |
| Make rs2275848(G;T) |
| Make rs2275848(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 9 |
| Position | 93125038 |
| Gene | NINJ1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs2275848 |
| dbSNP (classic) | rs2275848 |
| ClinGen | rs2275848 |
| ebi | rs2275848 |
| HLI | rs2275848 |
| Exac | rs2275848 |
| Gnomad | rs2275848 |
| Varsome | rs2275848 |
| LitVar | rs2275848 |
| Map | rs2275848 |
| PheGenI | rs2275848 |
| Biobank | rs2275848 |
| 1000 genomes | rs2275848 |
| hgdp | rs2275848 |
| ensembl | rs2275848 |
| geneview | rs2275848 |
| scholar | rs2275848 |
| rs2275848 | |
| pharmgkb | rs2275848 |
| gwascentral | rs2275848 |
| openSNP | rs2275848 |
| 23andMe | rs2275848 |
| SNPshot | rs2275848 |
| SNPdbe | rs2275848 |
| MSV3d | rs2275848 |
| GWAS Ctlg | rs2275848 |
| GMAF | 0.2048 |
| Max Magnitude | 0 |
| ? | (G;G) (G;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 | T |
| P-val | 1E-6 |
| Odds Ratio | 1.23 [1.13-1.34] |
