rs3826169
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs3826169(C;C) |
| Make rs3826169(C;T) |
| Make rs3826169(T;T) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 16 |
| Position | 53826569 |
| Gene | FTO |
| is a | snp |
| is | mentioned by |
| dbSNP | rs3826169 |
| dbSNP (classic) | rs3826169 |
| ClinGen | rs3826169 |
| ebi | rs3826169 |
| HLI | rs3826169 |
| Exac | rs3826169 |
| Gnomad | rs3826169 |
| Varsome | rs3826169 |
| LitVar | rs3826169 |
| Map | rs3826169 |
| PheGenI | rs3826169 |
| Biobank | rs3826169 |
| 1000 genomes | rs3826169 |
| hgdp | rs3826169 |
| ensembl | rs3826169 |
| geneview | rs3826169 |
| scholar | rs3826169 |
| rs3826169 | |
| pharmgkb | rs3826169 |
| gwascentral | rs3826169 |
| openSNP | rs3826169 |
| 23andMe | rs3826169 |
| SNPshot | rs3826169 |
| SNPdbe | rs3826169 |
| MSV3d | rs3826169 |
| GWAS Ctlg | rs3826169 |
| GMAF | 0.236 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 24289790
] Influence of FTO variants on obesity, inflammation and cardiovascular disease risk biomarkers in Spanish children: a case--control multicentre study
