rs2274432
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs2274432(C;C) |
| Make rs2274432(C;T) |
| Make rs2274432(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 1 |
| Position | 184051811 |
| Gene | COLGALT2, TSEN15 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs2274432 |
| dbSNP (classic) | rs2274432 |
| ClinGen | rs2274432 |
| ebi | rs2274432 |
| HLI | rs2274432 |
| Exac | rs2274432 |
| Gnomad | rs2274432 |
| Varsome | rs2274432 |
| LitVar | rs2274432 |
| Map | rs2274432 |
| PheGenI | rs2274432 |
| Biobank | rs2274432 |
| 1000 genomes | rs2274432 |
| hgdp | rs2274432 |
| ensembl | rs2274432 |
| geneview | rs2274432 |
| scholar | rs2274432 |
| rs2274432 | |
| pharmgkb | rs2274432 |
| gwascentral | rs2274432 |
| openSNP | rs2274432 |
| 23andMe | rs2274432 |
| SNPshot | rs2274432 |
| SNPdbe | rs2274432 |
| MSV3d | rs2274432 |
| GWAS Ctlg | rs2274432 |
| GMAF | 0.3223 |
| 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 | T |
| P-val | 8.0000000000000005E-9 |
| Odds Ratio | 5.30 [3.54-7.06] % SD taller |
[PMID 19474294
] Potential etiologic and functional implications of genome-wide association loci for human diseases and traits.
[PMID 20546612] The role of height-associated loci identified in genome wide association studies in the determination of pediatric stature.
