rs75596750
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs75596750(A;A) |
| Make rs75596750(A;G) |
| Make rs75596750(G;G) |
| Reference | GRCh38.p7 38.3/149 |
| Chromosome | 8 |
| Position | 134610608 |
| Gene | ZFAT |
| is a | snp |
| is | mentioned by |
| dbSNP | rs75596750 |
| dbSNP (classic) | rs75596750 |
| ClinGen | rs75596750 |
| ebi | rs75596750 |
| HLI | rs75596750 |
| Exac | rs75596750 |
| Gnomad | rs75596750 |
| Varsome | rs75596750 |
| LitVar | rs75596750 |
| Map | rs75596750 |
| PheGenI | rs75596750 |
| Biobank | rs75596750 |
| 1000 genomes | rs75596750 |
| hgdp | rs75596750 |
| ensembl | rs75596750 |
| geneview | rs75596750 |
| scholar | rs75596750 |
| rs75596750 | |
| pharmgkb | rs75596750 |
| gwascentral | rs75596750 |
| openSNP | rs75596750 |
| 23andMe | rs75596750 |
| SNPshot | rs75596750 |
| SNPdbe | rs75596750 |
| MSV3d | rs75596750 |
| GWAS Ctlg | rs75596750 |
| Max Magnitude | 0 |
[PMID 28146470
] Rare and low-frequency coding variants alter human adult height.
