rs3825199
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs3825199(C;C) |
| Make rs3825199(C;T) |
| Make rs3825199(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 12 |
| Position | 93583178 |
| Gene | SOCS2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs3825199 |
| dbSNP (classic) | rs3825199 |
| ClinGen | rs3825199 |
| ebi | rs3825199 |
| HLI | rs3825199 |
| Exac | rs3825199 |
| Gnomad | rs3825199 |
| Varsome | rs3825199 |
| LitVar | rs3825199 |
| Map | rs3825199 |
| PheGenI | rs3825199 |
| Biobank | rs3825199 |
| 1000 genomes | rs3825199 |
| hgdp | rs3825199 |
| ensembl | rs3825199 |
| geneview | rs3825199 |
| scholar | rs3825199 |
| rs3825199 | |
| pharmgkb | rs3825199 |
| gwascentral | rs3825199 |
| openSNP | rs3825199 |
| 23andMe | rs3825199 |
| SNPshot | rs3825199 |
| SNPdbe | rs3825199 |
| MSV3d | rs3825199 |
| GWAS Ctlg | rs3825199 |
| GMAF | 0.2608 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 18391951] |
| Trait | Height |
| Title | Many sequence variants affecting diversity of adult human height |
| Risk Allele | C |
| P-val | 1.9999999999999999E-7 |
| Odds Ratio | 6.20 [3.85-8.55] % SD taller |
[PMID 20546612
] The role of height-associated loci identified in genome wide association studies in the determination of pediatric stature.
