rs7652177
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs7652177(C;C) |
| Make rs7652177(C;G) |
| Make rs7652177(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 3 |
| Position | 172251287 |
| Gene | FNDC3B |
| is a | snp |
| is | mentioned by |
| dbSNP | rs7652177 |
| dbSNP (classic) | rs7652177 |
| ClinGen | rs7652177 |
| ebi | rs7652177 |
| HLI | rs7652177 |
| Exac | rs7652177 |
| Gnomad | rs7652177 |
| Varsome | rs7652177 |
| LitVar | rs7652177 |
| Map | rs7652177 |
| PheGenI | rs7652177 |
| Biobank | rs7652177 |
| 1000 genomes | rs7652177 |
| hgdp | rs7652177 |
| ensembl | rs7652177 |
| geneview | rs7652177 |
| scholar | rs7652177 |
| rs7652177 | |
| pharmgkb | rs7652177 |
| gwascentral | rs7652177 |
| openSNP | rs7652177 |
| 23andMe | rs7652177 |
| SNPshot | rs7652177 |
| SNPdbe | rs7652177 |
| MSV3d | rs7652177 |
| GWAS Ctlg | rs7652177 |
| GMAF | 0.3884 |
| Max Magnitude | 0 |
| ? | (C;C) (C;G) (G;G) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 20881960 ]
|
| Trait | Height |
| Title | Hundreds of variants clustered in genomic loci and biological pathways affect human height. |
| Risk Allele | |
| P-val | 7E-11 |
| Odds Ratio | NR NR |
