rs17480616
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs17480616(C;C) |
| Make rs17480616(C;G) |
| Make rs17480616(G;G) |
| Reference | GRCh38.p7 38.3/149 |
| Chromosome | 7 |
| Position | 135438312 |
| Gene | CNOT4 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs17480616 |
| dbSNP (classic) | rs17480616 |
| ClinGen | rs17480616 |
| ebi | rs17480616 |
| HLI | rs17480616 |
| Exac | rs17480616 |
| Gnomad | rs17480616 |
| Varsome | rs17480616 |
| LitVar | rs17480616 |
| Map | rs17480616 |
| PheGenI | rs17480616 |
| Biobank | rs17480616 |
| 1000 genomes | rs17480616 |
| hgdp | rs17480616 |
| ensembl | rs17480616 |
| geneview | rs17480616 |
| scholar | rs17480616 |
| rs17480616 | |
| pharmgkb | rs17480616 |
| gwascentral | rs17480616 |
| openSNP | rs17480616 |
| 23andMe | rs17480616 |
| SNPshot | rs17480616 |
| SNPdbe | rs17480616 |
| MSV3d | rs17480616 |
| GWAS Ctlg | rs17480616 |
| Max Magnitude | 0 |
| ? | (C;C) (C;G) (G;G) | 28 |
|---|---|---|
|
| ||
[PMID 28146470
] Rare and low-frequency coding variants alter human adult height.
