rs4713858
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs4713858(A;A) |
| Make rs4713858(A;G) |
| Make rs4713858(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 6 |
| Position | 35435008 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs4713858 |
| dbSNP (classic) | rs4713858 |
| ClinGen | rs4713858 |
| ebi | rs4713858 |
| HLI | rs4713858 |
| Exac | rs4713858 |
| Gnomad | rs4713858 |
| Varsome | rs4713858 |
| LitVar | rs4713858 |
| Map | rs4713858 |
| PheGenI | rs4713858 |
| Biobank | rs4713858 |
| 1000 genomes | rs4713858 |
| hgdp | rs4713858 |
| ensembl | rs4713858 |
| geneview | rs4713858 |
| scholar | rs4713858 |
| rs4713858 | |
| pharmgkb | rs4713858 |
| gwascentral | rs4713858 |
| openSNP | rs4713858 |
| 23andMe | rs4713858 |
| SNPshot | rs4713858 |
| SNPdbe | rs4713858 |
| MSV3d | rs4713858 |
| GWAS Ctlg | rs4713858 |
| GMAF | 0.152 |
| 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 | 4E-8 |
| Odds Ratio | 6.80 [4.45-9.15] % SD taller |
[PMID 19030899
] Genome-wide association scan for stature in Chinese: evidence for ethnic specific loci.
[PMID 19039035] Genome-wide association study identifies two novel loci containing FLNB and SBF2 genes underlying stature variation.
[PMID 20546612] The role of height-associated loci identified in genome wide association studies in the determination of pediatric stature.
