rs3208856
From SNPedia
					| Orientation | plus | 
| Stabilized | plus | 
| Make rs3208856(C;C) | 
| Make rs3208856(C;T) | 
| Make rs3208856(T;T) | 
| Reference | GRCh38.p7 38.3/149 | 
| Chromosome | 19 | 
| Position | 44793549 | 
| Gene | CBLC | 
| is a | snp | 
| is | mentioned by | 
| dbSNP | rs3208856 | 
| dbSNP (classic) | rs3208856 | 
| ClinGen | rs3208856 | 
| ebi | rs3208856 | 
| HLI | rs3208856 | 
| Exac | rs3208856 | 
| Gnomad | rs3208856 | 
| Varsome | rs3208856 | 
| LitVar | rs3208856 | 
| Map | rs3208856 | 
| PheGenI | rs3208856 | 
| Biobank | rs3208856 | 
| 1000 genomes | rs3208856 | 
| hgdp | rs3208856 | 
| ensembl | rs3208856 | 
| geneview | rs3208856 | 
| scholar | rs3208856 | 
| rs3208856 | |
| pharmgkb | rs3208856 | 
| gwascentral | rs3208856 | 
| openSNP | rs3208856 | 
| 23andMe | rs3208856 | 
| SNPshot | rs3208856 | 
| SNPdbe | rs3208856 | 
| MSV3d | rs3208856 | 
| GWAS Ctlg | rs3208856 | 
| Max Magnitude | 0 | 
| ? | (C;C) (C;T) (T;T) | 28 | 
|---|---|---|
| 
 
 | ||
[PMID 28146470 ] Rare and low-frequency coding variants alter human adult height.
] Rare and low-frequency coding variants alter human adult height.


