rs146301345
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs146301345(A;A) |
| Make rs146301345(A;G) |
| Make rs146301345(G;G) |
| Reference | GRCh38.p7 38.3/149 |
| Chromosome | 5 |
| Position | 32784801 |
| Gene | NPR3 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs146301345 |
| dbSNP (classic) | rs146301345 |
| ClinGen | rs146301345 |
| ebi | rs146301345 |
| HLI | rs146301345 |
| Exac | rs146301345 |
| Gnomad | rs146301345 |
| Varsome | rs146301345 |
| LitVar | rs146301345 |
| Map | rs146301345 |
| PheGenI | rs146301345 |
| Biobank | rs146301345 |
| 1000 genomes | rs146301345 |
| hgdp | rs146301345 |
| ensembl | rs146301345 |
| geneview | rs146301345 |
| scholar | rs146301345 |
| rs146301345 | |
| pharmgkb | rs146301345 |
| gwascentral | rs146301345 |
| openSNP | rs146301345 |
| 23andMe | rs146301345 |
| SNPshot | rs146301345 |
| SNPdbe | rs146301345 |
| MSV3d | rs146301345 |
| GWAS Ctlg | rs146301345 |
| Max Magnitude | 0 |
[PMID 28146470
] Rare and low-frequency coding variants alter human adult height.
