rs41291604
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs41291604(A;A) |
| Make rs41291604(A;G) |
| Make rs41291604(G;G) |
| Reference | GRCh38.p7 38.3/149 |
| Chromosome | 10 |
| Position | 96159254 |
| Gene | ZNF518A |
| is a | snp |
| is | mentioned by |
| dbSNP | rs41291604 |
| dbSNP (classic) | rs41291604 |
| ClinGen | rs41291604 |
| ebi | rs41291604 |
| HLI | rs41291604 |
| Exac | rs41291604 |
| Gnomad | rs41291604 |
| Varsome | rs41291604 |
| LitVar | rs41291604 |
| Map | rs41291604 |
| PheGenI | rs41291604 |
| Biobank | rs41291604 |
| 1000 genomes | rs41291604 |
| hgdp | rs41291604 |
| ensembl | rs41291604 |
| geneview | rs41291604 |
| scholar | rs41291604 |
| rs41291604 | |
| pharmgkb | rs41291604 |
| gwascentral | rs41291604 |
| openSNP | rs41291604 |
| 23andMe | rs41291604 |
| SNPshot | rs41291604 |
| SNPdbe | rs41291604 |
| MSV3d | rs41291604 |
| GWAS Ctlg | rs41291604 |
| Max Magnitude | 0 |
[PMID 28146470
] Rare and low-frequency coding variants alter human adult height.
