rs5757949
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs5757949(C;C) |
| Make rs5757949(C;T) |
| Make rs5757949(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 22 |
| Position | 40424147 |
| Gene | MKL1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs5757949 |
| dbSNP (classic) | rs5757949 |
| ClinGen | rs5757949 |
| ebi | rs5757949 |
| HLI | rs5757949 |
| Exac | rs5757949 |
| Gnomad | rs5757949 |
| Varsome | rs5757949 |
| LitVar | rs5757949 |
| Map | rs5757949 |
| PheGenI | rs5757949 |
| Biobank | rs5757949 |
| 1000 genomes | rs5757949 |
| hgdp | rs5757949 |
| ensembl | rs5757949 |
| geneview | rs5757949 |
| scholar | rs5757949 |
| rs5757949 | |
| pharmgkb | rs5757949 |
| gwascentral | rs5757949 |
| openSNP | rs5757949 |
| 23andMe | rs5757949 |
| SNPshot | rs5757949 |
| SNPdbe | rs5757949 |
| MSV3d | rs5757949 |
| GWAS Ctlg | rs5757949 |
| GMAF | 0.2388 |
| 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 | 0.000004 |
| Odds Ratio | NR NR |
