rs4252548
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs4252548(A;A) |
| Make rs4252548(A;G) |
| Make rs4252548(G;G) |
| Reference | GRCh38.p7 38.3/149 |
| Chromosome | 19 |
| Position | 55368304 |
| Gene | IL11 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs4252548 |
| dbSNP (classic) | rs4252548 |
| ClinGen | rs4252548 |
| ebi | rs4252548 |
| HLI | rs4252548 |
| Exac | rs4252548 |
| Gnomad | rs4252548 |
| Varsome | rs4252548 |
| LitVar | rs4252548 |
| Map | rs4252548 |
| PheGenI | rs4252548 |
| Biobank | rs4252548 |
| 1000 genomes | rs4252548 |
| hgdp | rs4252548 |
| ensembl | rs4252548 |
| geneview | rs4252548 |
| scholar | rs4252548 |
| rs4252548 | |
| pharmgkb | rs4252548 |
| gwascentral | rs4252548 |
| openSNP | rs4252548 |
| 23andMe | rs4252548 |
| SNPshot | rs4252548 |
| SNPdbe | rs4252548 |
| MSV3d | rs4252548 |
| GWAS Ctlg | rs4252548 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
[PMID 28146470
] Rare and low-frequency coding variants alter human adult height.
