rs7187365
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs7187365(C;C) |
| Make rs7187365(C;T) |
| Make rs7187365(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 16 |
| Position | 86478309 |
| Gene | FENDRR |
| is a | snp |
| is | mentioned by |
| dbSNP | rs7187365 |
| dbSNP (classic) | rs7187365 |
| ClinGen | rs7187365 |
| ebi | rs7187365 |
| HLI | rs7187365 |
| Exac | rs7187365 |
| Gnomad | rs7187365 |
| Varsome | rs7187365 |
| LitVar | rs7187365 |
| Map | rs7187365 |
| PheGenI | rs7187365 |
| Biobank | rs7187365 |
| 1000 genomes | rs7187365 |
| hgdp | rs7187365 |
| ensembl | rs7187365 |
| geneview | rs7187365 |
| scholar | rs7187365 |
| rs7187365 | |
| pharmgkb | rs7187365 |
| gwascentral | rs7187365 |
| openSNP | rs7187365 |
| 23andMe | rs7187365 |
| SNPshot | rs7187365 |
| SNPdbe | rs7187365 |
| MSV3d | rs7187365 |
| GWAS Ctlg | rs7187365 |
| GMAF | 0.1901 |
| 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 | 6E-6 |
| Odds Ratio | 1.22 [1.12-1.33] |
