rs34471628
From SNPedia
					| Orientation | minus | 
| Stabilized | minus | 
| Make rs34471628(C;C) | 
| Make rs34471628(C;T) | 
| Make rs34471628(T;T) | 
| Reference | GRCh38.p7 38.3/149 | 
| Chromosome | 5 | 
| Position | 172769749 | 
| Gene | DUSP1 | 
| is a | snp | 
| is | mentioned by | 
| dbSNP | rs34471628 | 
| dbSNP (classic) | rs34471628 | 
| ClinGen | rs34471628 | 
| ebi | rs34471628 | 
| HLI | rs34471628 | 
| Exac | rs34471628 | 
| Gnomad | rs34471628 | 
| Varsome | rs34471628 | 
| LitVar | rs34471628 | 
| Map | rs34471628 | 
| PheGenI | rs34471628 | 
| Biobank | rs34471628 | 
| 1000 genomes | rs34471628 | 
| hgdp | rs34471628 | 
| ensembl | rs34471628 | 
| geneview | rs34471628 | 
| scholar | rs34471628 | 
| rs34471628 | |
| pharmgkb | rs34471628 | 
| gwascentral | rs34471628 | 
| openSNP | rs34471628 | 
| 23andMe | rs34471628 | 
| SNPshot | rs34471628 | 
| SNPdbe | rs34471628 | 
| MSV3d | rs34471628 | 
| GWAS Ctlg | rs34471628 | 
| 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.


