rs1631486
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs1631486(C;C) |
| Make rs1631486(C;T) |
| Make rs1631486(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 18 |
| Position | 55359126 |
| Gene | TCF4 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1631486 |
| dbSNP (classic) | rs1631486 |
| ClinGen | rs1631486 |
| ebi | rs1631486 |
| HLI | rs1631486 |
| Exac | rs1631486 |
| Gnomad | rs1631486 |
| Varsome | rs1631486 |
| LitVar | rs1631486 |
| Map | rs1631486 |
| PheGenI | rs1631486 |
| Biobank | rs1631486 |
| 1000 genomes | rs1631486 |
| hgdp | rs1631486 |
| ensembl | rs1631486 |
| geneview | rs1631486 |
| scholar | rs1631486 |
| rs1631486 | |
| pharmgkb | rs1631486 |
| gwascentral | rs1631486 |
| openSNP | rs1631486 |
| 23andMe | rs1631486 |
| SNPshot | rs1631486 |
| SNPdbe | rs1631486 |
| MSV3d | rs1631486 |
| GWAS Ctlg | rs1631486 |
| GMAF | 0.4858 |
| 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 | A |
| P-val | 4E-6 |
| Odds Ratio | 1.18 [1.10-1.26] |
