rs79485039
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs79485039(C;C) |
| Make rs79485039(C;T) |
| Make rs79485039(T;T) |
| Reference | GRCh38.p7 38.3/149 |
| Chromosome | 1 |
| Position | 180917004 |
| Gene | KIAA1614 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs79485039 |
| dbSNP (classic) | rs79485039 |
| ClinGen | rs79485039 |
| ebi | rs79485039 |
| HLI | rs79485039 |
| Exac | rs79485039 |
| Gnomad | rs79485039 |
| Varsome | rs79485039 |
| LitVar | rs79485039 |
| Map | rs79485039 |
| PheGenI | rs79485039 |
| Biobank | rs79485039 |
| 1000 genomes | rs79485039 |
| hgdp | rs79485039 |
| ensembl | rs79485039 |
| geneview | rs79485039 |
| scholar | rs79485039 |
| rs79485039 | |
| pharmgkb | rs79485039 |
| gwascentral | rs79485039 |
| openSNP | rs79485039 |
| 23andMe | rs79485039 |
| SNPshot | rs79485039 |
| SNPdbe | rs79485039 |
| MSV3d | rs79485039 |
| GWAS Ctlg | rs79485039 |
| Max Magnitude | 0 |
[PMID 28146470
] Rare and low-frequency coding variants alter human adult height.
