rs145659444
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs145659444(C;C) |
| Make rs145659444(C;T) |
| Make rs145659444(T;T) |
| Reference | GRCh38.p7 38.3/149 |
| Chromosome | 1 |
| Position | 149930450 |
| Gene | MTMR11 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs145659444 |
| dbSNP (classic) | rs145659444 |
| ClinGen | rs145659444 |
| ebi | rs145659444 |
| HLI | rs145659444 |
| Exac | rs145659444 |
| Gnomad | rs145659444 |
| Varsome | rs145659444 |
| LitVar | rs145659444 |
| Map | rs145659444 |
| PheGenI | rs145659444 |
| Biobank | rs145659444 |
| 1000 genomes | rs145659444 |
| hgdp | rs145659444 |
| ensembl | rs145659444 |
| geneview | rs145659444 |
| scholar | rs145659444 |
| rs145659444 | |
| pharmgkb | rs145659444 |
| gwascentral | rs145659444 |
| openSNP | rs145659444 |
| 23andMe | rs145659444 |
| SNPshot | rs145659444 |
| SNPdbe | rs145659444 |
| MSV3d | rs145659444 |
| GWAS Ctlg | rs145659444 |
| Max Magnitude | 0 |
[PMID 28146470
] Rare and low-frequency coding variants alter human adult height.
