rs1239947
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs1239947(A;A) |
| Make rs1239947(A;G) |
| Make rs1239947(G;G) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 13 |
| Position | 50532419 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1239947 |
| dbSNP (classic) | rs1239947 |
| ClinGen | rs1239947 |
| ebi | rs1239947 |
| HLI | rs1239947 |
| Exac | rs1239947 |
| Gnomad | rs1239947 |
| Varsome | rs1239947 |
| LitVar | rs1239947 |
| Map | rs1239947 |
| PheGenI | rs1239947 |
| Biobank | rs1239947 |
| 1000 genomes | rs1239947 |
| hgdp | rs1239947 |
| ensembl | rs1239947 |
| geneview | rs1239947 |
| scholar | rs1239947 |
| rs1239947 | |
| pharmgkb | rs1239947 |
| gwascentral | rs1239947 |
| openSNP | rs1239947 |
| 23andMe | rs1239947 |
| SNPshot | rs1239947 |
| SNPdbe | rs1239947 |
| MSV3d | rs1239947 |
| GWAS Ctlg | rs1239947 |
| GMAF | 0.2548 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 18391951] |
| Trait | Height |
| Title | Many sequence variants affecting diversity of adult human height |
| Risk Allele | G |
| P-val | 0.0000079999999999999996 |
| Odds Ratio | 3.80 [2.23-5.37] % SD taller |
[PMID 20546612
] The role of height-associated loci identified in genome wide association studies in the determination of pediatric stature.
