rs148543891
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs148543891(A;A) |
| Make rs148543891(A;G) |
| Make rs148543891(G;G) |
| Reference | GRCh38.p7 38.3/149 |
| Chromosome | 6 |
| Position | 155129645 |
| Gene | TIAM2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs148543891 |
| dbSNP (classic) | rs148543891 |
| ClinGen | rs148543891 |
| ebi | rs148543891 |
| HLI | rs148543891 |
| Exac | rs148543891 |
| Gnomad | rs148543891 |
| Varsome | rs148543891 |
| LitVar | rs148543891 |
| Map | rs148543891 |
| PheGenI | rs148543891 |
| Biobank | rs148543891 |
| 1000 genomes | rs148543891 |
| hgdp | rs148543891 |
| ensembl | rs148543891 |
| geneview | rs148543891 |
| scholar | rs148543891 |
| rs148543891 | |
| pharmgkb | rs148543891 |
| gwascentral | rs148543891 |
| openSNP | rs148543891 |
| 23andMe | rs148543891 |
| SNPshot | rs148543891 |
| SNPdbe | rs148543891 |
| MSV3d | rs148543891 |
| GWAS Ctlg | rs148543891 |
| Max Magnitude | 0 |
[PMID 28146470
] Rare and low-frequency coding variants alter human adult height.
