rs77885044
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs77885044(C;C) |
| Make rs77885044(C;T) |
| Make rs77885044(T;T) |
| Reference | GRCh38.p7 38.3/149 |
| Chromosome | 22 |
| Position | 28105426 |
| Gene | TTC28 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs77885044 |
| dbSNP (classic) | rs77885044 |
| ClinGen | rs77885044 |
| ebi | rs77885044 |
| HLI | rs77885044 |
| Exac | rs77885044 |
| Gnomad | rs77885044 |
| Varsome | rs77885044 |
| LitVar | rs77885044 |
| Map | rs77885044 |
| PheGenI | rs77885044 |
| Biobank | rs77885044 |
| 1000 genomes | rs77885044 |
| hgdp | rs77885044 |
| ensembl | rs77885044 |
| geneview | rs77885044 |
| scholar | rs77885044 |
| rs77885044 | |
| pharmgkb | rs77885044 |
| gwascentral | rs77885044 |
| openSNP | rs77885044 |
| 23andMe | rs77885044 |
| SNPshot | rs77885044 |
| SNPdbe | rs77885044 |
| MSV3d | rs77885044 |
| GWAS Ctlg | rs77885044 |
| Max Magnitude | 0 |
[PMID 28146470
] Rare and low-frequency coding variants alter human adult height.
