rs9941349
| Orientation | plus |
| Stabilized | plus |
| Make rs9941349(C;C) |
| Make rs9941349(C;T) |
| Make rs9941349(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 16 |
| Position | 53791576 |
| Gene | FTO |
| is a | snp |
| is | mentioned by |
| dbSNP | rs9941349 |
| dbSNP (classic) | rs9941349 |
| ClinGen | rs9941349 |
| ebi | rs9941349 |
| HLI | rs9941349 |
| Exac | rs9941349 |
| Gnomad | rs9941349 |
| Varsome | rs9941349 |
| LitVar | rs9941349 |
| Map | rs9941349 |
| PheGenI | rs9941349 |
| Biobank | rs9941349 |
| 1000 genomes | rs9941349 |
| hgdp | rs9941349 |
| ensembl | rs9941349 |
| geneview | rs9941349 |
| scholar | rs9941349 |
| rs9941349 | |
| pharmgkb | rs9941349 |
| gwascentral | rs9941349 |
| openSNP | rs9941349 |
| 23andMe | rs9941349 |
| SNPshot | rs9941349 |
| SNPdbe | rs9941349 |
| MSV3d | rs9941349 |
| GWAS Ctlg | rs9941349 |
| GMAF | 0.2833 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 19553259 ]
|
| Trait | Obesity (extreme) |
| Title | Common BMI-associated variants confer risk of extreme obesity |
| Risk Allele | T |
| P-val | 6E-12 |
| Odds Ratio | 1.48 [1.33-1.66] |
[PMID 20430937] Fine-mapping of the association with obesity at the FTO locus in African-derived populations
[PMID 18335027] Association analysis of the FTO gene with obesity in children of Caucasian and African ancestry reveals a common tagging SNP.
[PMID 20442772] Common SNPs in FTO gene are associated with obesity related anthropometric traits in an island population from the eastern Adriatic coast of Croatia.
[PMID 25177340] Phenome-wide association studies demonstrating pleiotropy of genetic variants within FTO with and without adjustment for body mass index
[PMID 32384785] Applicability of Obesity-Related SNPs and their Effect Size Measures Defined on Populations with European Ancestry for Genetic Risk Estimation among Roma.
