rs35658696
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs35658696(C;C) |
| Make rs35658696(C;T) |
| Make rs35658696(T;T) |
| Reference | GRCh38.p7 38.3/149 |
| Chromosome | 5 |
| Position | 103003107 |
| Gene | PAM |
| is a | snp |
| is | mentioned by |
| dbSNP | rs35658696 |
| dbSNP (classic) | rs35658696 |
| ClinGen | rs35658696 |
| ebi | rs35658696 |
| HLI | rs35658696 |
| Exac | rs35658696 |
| Gnomad | rs35658696 |
| Varsome | rs35658696 |
| LitVar | rs35658696 |
| Map | rs35658696 |
| PheGenI | rs35658696 |
| Biobank | rs35658696 |
| 1000 genomes | rs35658696 |
| hgdp | rs35658696 |
| ensembl | rs35658696 |
| geneview | rs35658696 |
| scholar | rs35658696 |
| rs35658696 | |
| pharmgkb | rs35658696 |
| gwascentral | rs35658696 |
| openSNP | rs35658696 |
| 23andMe | rs35658696 |
| SNPshot | rs35658696 |
| SNPdbe | rs35658696 |
| MSV3d | rs35658696 |
| GWAS Ctlg | rs35658696 |
| Max Magnitude | 0 |
[PMID 28146470
] Rare and low-frequency coding variants alter human adult height.
