rs150494621
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs150494621(C;C) |
| Make rs150494621(C;T) |
| Make rs150494621(T;T) |
| Reference | GRCh38.p7 38.3/149 |
| Chromosome | 15 |
| Position | 43861373 |
| Gene | WDR76 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs150494621 |
| dbSNP (classic) | rs150494621 |
| ClinGen | rs150494621 |
| ebi | rs150494621 |
| HLI | rs150494621 |
| Exac | rs150494621 |
| Gnomad | rs150494621 |
| Varsome | rs150494621 |
| LitVar | rs150494621 |
| Map | rs150494621 |
| PheGenI | rs150494621 |
| Biobank | rs150494621 |
| 1000 genomes | rs150494621 |
| hgdp | rs150494621 |
| ensembl | rs150494621 |
| geneview | rs150494621 |
| scholar | rs150494621 |
| rs150494621 | |
| pharmgkb | rs150494621 |
| gwascentral | rs150494621 |
| openSNP | rs150494621 |
| 23andMe | rs150494621 |
| SNPshot | rs150494621 |
| SNPdbe | rs150494621 |
| MSV3d | rs150494621 |
| GWAS Ctlg | rs150494621 |
| Max Magnitude | 0 |
[PMID 28146470
] Rare and low-frequency coding variants alter human adult height.
