rs147110934
From SNPedia
					| Orientation | plus | 
| Stabilized | plus | 
| Make rs147110934(G;G) | 
| Make rs147110934(G;T) | 
| Make rs147110934(T;T) | 
| Reference | GRCh38.p7 38.3/149 | 
| Chromosome | 19 | 
| Position | 55482069 | 
| Gene | ZNF628 | 
| is a | snp | 
| is | mentioned by | 
| dbSNP | rs147110934 | 
| dbSNP (classic) | rs147110934 | 
| ClinGen | rs147110934 | 
| ebi | rs147110934 | 
| HLI | rs147110934 | 
| Exac | rs147110934 | 
| Gnomad | rs147110934 | 
| Varsome | rs147110934 | 
| LitVar | rs147110934 | 
| Map | rs147110934 | 
| PheGenI | rs147110934 | 
| Biobank | rs147110934 | 
| 1000 genomes | rs147110934 | 
| hgdp | rs147110934 | 
| ensembl | rs147110934 | 
| geneview | rs147110934 | 
| scholar | rs147110934 | 
| rs147110934 | |
| pharmgkb | rs147110934 | 
| gwascentral | rs147110934 | 
| openSNP | rs147110934 | 
| 23andMe | rs147110934 | 
| SNPshot | rs147110934 | 
| SNPdbe | rs147110934 | 
| MSV3d | rs147110934 | 
| GWAS Ctlg | rs147110934 | 
| Max Magnitude | 0 | 
[PMID 28146470 ] Rare and low-frequency coding variants alter human adult height.
] Rare and low-frequency coding variants alter human adult height.


