rs113388806
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs113388806(A;A) |
| Make rs113388806(A;T) |
| Make rs113388806(T;T) |
| Reference | GRCh38.p7 38.3/149 |
| Chromosome | 16 |
| Position | 24793633 |
| Gene | TNRC6A |
| is a | snp |
| is | mentioned by |
| dbSNP | rs113388806 |
| dbSNP (classic) | rs113388806 |
| ClinGen | rs113388806 |
| ebi | rs113388806 |
| HLI | rs113388806 |
| Exac | rs113388806 |
| Gnomad | rs113388806 |
| Varsome | rs113388806 |
| LitVar | rs113388806 |
| Map | rs113388806 |
| PheGenI | rs113388806 |
| Biobank | rs113388806 |
| 1000 genomes | rs113388806 |
| hgdp | rs113388806 |
| ensembl | rs113388806 |
| geneview | rs113388806 |
| scholar | rs113388806 |
| rs113388806 | |
| pharmgkb | rs113388806 |
| gwascentral | rs113388806 |
| openSNP | rs113388806 |
| 23andMe | rs113388806 |
| SNPshot | rs113388806 |
| SNPdbe | rs113388806 |
| MSV3d | rs113388806 |
| GWAS Ctlg | rs113388806 |
| Max Magnitude | 0 |
[PMID 28146470
] Rare and low-frequency coding variants alter human adult height.
