rs117801489
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs117801489(C;C) |
| Make rs117801489(C;T) |
| Make rs117801489(T;T) |
| Reference | GRCh38.p7 38.3/149 |
| Chromosome | 12 |
| Position | 104015054 |
| Gene | GLT8D2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs117801489 |
| dbSNP (classic) | rs117801489 |
| ClinGen | rs117801489 |
| ebi | rs117801489 |
| HLI | rs117801489 |
| Exac | rs117801489 |
| Gnomad | rs117801489 |
| Varsome | rs117801489 |
| LitVar | rs117801489 |
| Map | rs117801489 |
| PheGenI | rs117801489 |
| Biobank | rs117801489 |
| 1000 genomes | rs117801489 |
| hgdp | rs117801489 |
| ensembl | rs117801489 |
| geneview | rs117801489 |
| scholar | rs117801489 |
| rs117801489 | |
| pharmgkb | rs117801489 |
| gwascentral | rs117801489 |
| openSNP | rs117801489 |
| 23andMe | rs117801489 |
| SNPshot | rs117801489 |
| SNPdbe | rs117801489 |
| MSV3d | rs117801489 |
| GWAS Ctlg | rs117801489 |
| Max Magnitude | 0 |
[PMID 28146470
] Rare and low-frequency coding variants alter human adult height.
