rs11208659
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs11208659(C;C) |
| Make rs11208659(C;T) |
| Make rs11208659(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 1 |
| Position | 65513597 |
| Gene | LEPR |
| is a | snp |
| is | mentioned by |
| dbSNP | rs11208659 |
| dbSNP (classic) | rs11208659 |
| ClinGen | rs11208659 |
| ebi | rs11208659 |
| HLI | rs11208659 |
| Exac | rs11208659 |
| Gnomad | rs11208659 |
| Varsome | rs11208659 |
| LitVar | rs11208659 |
| Map | rs11208659 |
| PheGenI | rs11208659 |
| Biobank | rs11208659 |
| 1000 genomes | rs11208659 |
| hgdp | rs11208659 |
| ensembl | rs11208659 |
| geneview | rs11208659 |
| scholar | rs11208659 |
| rs11208659 | |
| pharmgkb | rs11208659 |
| gwascentral | rs11208659 |
| openSNP | rs11208659 |
| 23andMe | rs11208659 |
| SNPshot | rs11208659 |
| SNPdbe | rs11208659 |
| MSV3d | rs11208659 |
| GWAS Ctlg | rs11208659 |
| GMAF | 0.1556 |
| 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 | 2E-9 |
| Odds Ratio | 1.42 [1.27-1.59] |
[PMID 28771179] Leptin Receptor Gene Variant rs11804091 Is Associated with BMI and Insulin Resistance in Spanish Female Obese Children: A Case-Control Study.
