rs61733564
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs61733564(A;A) |
| Make rs61733564(A;G) |
| Make rs61733564(G;G) |
| Reference | GRCh38.p7 38.3/149 |
| Chromosome | 16 |
| Position | 4762704 |
| Gene | ZNF500 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs61733564 |
| dbSNP (classic) | rs61733564 |
| ClinGen | rs61733564 |
| ebi | rs61733564 |
| HLI | rs61733564 |
| Exac | rs61733564 |
| Gnomad | rs61733564 |
| Varsome | rs61733564 |
| LitVar | rs61733564 |
| Map | rs61733564 |
| PheGenI | rs61733564 |
| Biobank | rs61733564 |
| 1000 genomes | rs61733564 |
| hgdp | rs61733564 |
| ensembl | rs61733564 |
| geneview | rs61733564 |
| scholar | rs61733564 |
| rs61733564 | |
| pharmgkb | rs61733564 |
| gwascentral | rs61733564 |
| openSNP | rs61733564 |
| 23andMe | rs61733564 |
| SNPshot | rs61733564 |
| SNPdbe | rs61733564 |
| MSV3d | rs61733564 |
| GWAS Ctlg | rs61733564 |
| Max Magnitude | 0 |
[PMID 28146470
] Rare and low-frequency coding variants alter human adult height.
