rs147348682
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs147348682(G;G) |
| Make rs147348682(G;T) |
| Make rs147348682(T;T) |
| Reference | GRCh38.p7 38.3/149 |
| Chromosome | 22 |
| Position | 41699654 |
| Gene | MEI1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs147348682 |
| dbSNP (classic) | rs147348682 |
| ClinGen | rs147348682 |
| ebi | rs147348682 |
| HLI | rs147348682 |
| Exac | rs147348682 |
| Gnomad | rs147348682 |
| Varsome | rs147348682 |
| LitVar | rs147348682 |
| Map | rs147348682 |
| PheGenI | rs147348682 |
| Biobank | rs147348682 |
| 1000 genomes | rs147348682 |
| hgdp | rs147348682 |
| ensembl | rs147348682 |
| geneview | rs147348682 |
| scholar | rs147348682 |
| rs147348682 | |
| pharmgkb | rs147348682 |
| gwascentral | rs147348682 |
| openSNP | rs147348682 |
| 23andMe | rs147348682 |
| SNPshot | rs147348682 |
| SNPdbe | rs147348682 |
| MSV3d | rs147348682 |
| GWAS Ctlg | rs147348682 |
| Max Magnitude | 0 |
[PMID 28146470
] Rare and low-frequency coding variants alter human adult height.
