rs10472828
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs10472828(C;C) |
| Make rs10472828(C;T) |
| Make rs10472828(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 5 |
| Position | 32888712 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs10472828 |
| dbSNP (classic) | rs10472828 |
| ClinGen | rs10472828 |
| ebi | rs10472828 |
| HLI | rs10472828 |
| Exac | rs10472828 |
| Gnomad | rs10472828 |
| Varsome | rs10472828 |
| LitVar | rs10472828 |
| Map | rs10472828 |
| PheGenI | rs10472828 |
| Biobank | rs10472828 |
| 1000 genomes | rs10472828 |
| hgdp | rs10472828 |
| ensembl | rs10472828 |
| geneview | rs10472828 |
| scholar | rs10472828 |
| rs10472828 | |
| pharmgkb | rs10472828 |
| gwascentral | rs10472828 |
| openSNP | rs10472828 |
| 23andMe | rs10472828 |
| SNPshot | rs10472828 |
| SNPdbe | rs10472828 |
| MSV3d | rs10472828 |
| GWAS Ctlg | rs10472828 |
| GMAF | 0.4178 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 19343178 ]
|
| Trait | Height |
| Title | Meta-analysis of genome-wide scans for human adult stature identifies novel Loci and associations with measures of skeletal frame size |
| Risk Allele | |
| P-val | 3E-7 |
| Odds Ratio | |
[PMID 19570815] A genome-wide association study of northwestern Europeans involves the CNP signaling pathway in the etiology of human height variation
[PMID 20546612] The role of height-associated loci identified in genome wide association studies in the determination of pediatric stature.
