rs148833559
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (A;C) | 2 | Height-related; on average, 2cm taller than non-carriers |
| (C;C) | 0 | common/normal |
| Make rs148833559(A;A) |
| Reference | GRCh38.p7 38.3/149 |
| Chromosome | 5 |
| Position | 173328063 |
| Gene | STC2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs148833559 |
| dbSNP (classic) | rs148833559 |
| ClinGen | rs148833559 |
| ebi | rs148833559 |
| HLI | rs148833559 |
| Exac | rs148833559 |
| Gnomad | rs148833559 |
| Varsome | rs148833559 |
| LitVar | rs148833559 |
| Map | rs148833559 |
| PheGenI | rs148833559 |
| Biobank | rs148833559 |
| 1000 genomes | rs148833559 |
| hgdp | rs148833559 |
| ensembl | rs148833559 |
| geneview | rs148833559 |
| scholar | rs148833559 |
| rs148833559 | |
| pharmgkb | rs148833559 |
| gwascentral | rs148833559 |
| openSNP | rs148833559 |
| 23andMe | rs148833559 |
| SNPshot | rs148833559 |
| SNPdbe | rs148833559 |
| MSV3d | rs148833559 |
| GWAS Ctlg | rs148833559 |
| Max Magnitude | 2 |
[PMID 28146470
] Rare and low-frequency coding variants alter human adult height.
- Height related SNP; carriers of the (rare) minor allele for this STC2 gene missense variant are approximately 2.1cm taller than non-carriers.
