rs139909
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs139909(C;C) |
| Make rs139909(C;T) |
| Make rs139909(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 22 |
| Position | 40301577 |
| Gene | TNRC6B |
| is a | snp |
| is | mentioned by |
| dbSNP | rs139909 |
| dbSNP (classic) | rs139909 |
| ClinGen | rs139909 |
| ebi | rs139909 |
| HLI | rs139909 |
| Exac | rs139909 |
| Gnomad | rs139909 |
| Varsome | rs139909 |
| LitVar | rs139909 |
| Map | rs139909 |
| PheGenI | rs139909 |
| Biobank | rs139909 |
| 1000 genomes | rs139909 |
| hgdp | rs139909 |
| ensembl | rs139909 |
| geneview | rs139909 |
| scholar | rs139909 |
| rs139909 | |
| pharmgkb | rs139909 |
| gwascentral | rs139909 |
| openSNP | rs139909 |
| 23andMe | rs139909 |
| SNPshot | rs139909 |
| SNPdbe | rs139909 |
| MSV3d | rs139909 |
| GWAS Ctlg | rs139909 |
| GMAF | 0.3186 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 19570815 ]
|
| Trait | Height |
| Title | A genome-wide association study of northwestern Europeans involves the CNP signaling pathway in the etiology of human height variation |
| Risk Allele | T |
| P-val | 2E-7 |
| Odds Ratio | 0.25 [0.03-0.47] cm increase |
