rs921122
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs921122(C;C) |
| Make rs921122(C;T) |
| Make rs921122(T;T) |
| Reference | GRCh38.p7 38.3/149 |
| Chromosome | 9 |
| Position | 92301665 |
| Gene | NOL8 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs921122 |
| dbSNP (classic) | rs921122 |
| ClinGen | rs921122 |
| ebi | rs921122 |
| HLI | rs921122 |
| Exac | rs921122 |
| Gnomad | rs921122 |
| Varsome | rs921122 |
| LitVar | rs921122 |
| Map | rs921122 |
| PheGenI | rs921122 |
| Biobank | rs921122 |
| 1000 genomes | rs921122 |
| hgdp | rs921122 |
| ensembl | rs921122 |
| geneview | rs921122 |
| scholar | rs921122 |
| rs921122 | |
| pharmgkb | rs921122 |
| gwascentral | rs921122 |
| openSNP | rs921122 |
| 23andMe | rs921122 |
| SNPshot | rs921122 |
| SNPdbe | rs921122 |
| MSV3d | rs921122 |
| GWAS Ctlg | rs921122 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 28146470
] Rare and low-frequency coding variants alter human adult height.
