rs4072796
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs4072796(C;C) |
| Make rs4072796(C;G) |
| Make rs4072796(G;G) |
| Reference | GRCh38.p7 38.3/149 |
| Chromosome | 12 |
| Position | 7396400 |
| Gene | CD163L1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs4072796 |
| dbSNP (classic) | rs4072796 |
| ClinGen | rs4072796 |
| ebi | rs4072796 |
| HLI | rs4072796 |
| Exac | rs4072796 |
| Gnomad | rs4072796 |
| Varsome | rs4072796 |
| LitVar | rs4072796 |
| Map | rs4072796 |
| PheGenI | rs4072796 |
| Biobank | rs4072796 |
| 1000 genomes | rs4072796 |
| hgdp | rs4072796 |
| ensembl | rs4072796 |
| geneview | rs4072796 |
| scholar | rs4072796 |
| rs4072796 | |
| pharmgkb | rs4072796 |
| gwascentral | rs4072796 |
| openSNP | rs4072796 |
| 23andMe | rs4072796 |
| SNPshot | rs4072796 |
| SNPdbe | rs4072796 |
| MSV3d | rs4072796 |
| GWAS Ctlg | rs4072796 |
| Max Magnitude | 0 |
| ? | (C;C) (C;G) (G;G) | 28 |
|---|---|---|
|
| ||
[PMID 28146470
] Rare and low-frequency coding variants alter human adult height.
