rs117295933
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs117295933(A;A) |
| Make rs117295933(A;C) |
| Make rs117295933(C;C) |
| Reference | GRCh38.p7 38.3/149 |
| Chromosome | 14 |
| Position | 44934496 |
| Gene | KLHL28 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs117295933 |
| dbSNP (classic) | rs117295933 |
| ClinGen | rs117295933 |
| ebi | rs117295933 |
| HLI | rs117295933 |
| Exac | rs117295933 |
| Gnomad | rs117295933 |
| Varsome | rs117295933 |
| LitVar | rs117295933 |
| Map | rs117295933 |
| PheGenI | rs117295933 |
| Biobank | rs117295933 |
| 1000 genomes | rs117295933 |
| hgdp | rs117295933 |
| ensembl | rs117295933 |
| geneview | rs117295933 |
| scholar | rs117295933 |
| rs117295933 | |
| pharmgkb | rs117295933 |
| gwascentral | rs117295933 |
| openSNP | rs117295933 |
| 23andMe | rs117295933 |
| SNPshot | rs117295933 |
| SNPdbe | rs117295933 |
| MSV3d | rs117295933 |
| GWAS Ctlg | rs117295933 |
| Max Magnitude | 0 |
[PMID 28146470
] Rare and low-frequency coding variants alter human adult height.
