rs9360921
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs9360921(G;G) |
| Make rs9360921(G;T) |
| Make rs9360921(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 6 |
| Position | 75555926 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs9360921 |
| dbSNP (classic) | rs9360921 |
| ClinGen | rs9360921 |
| ebi | rs9360921 |
| HLI | rs9360921 |
| Exac | rs9360921 |
| Gnomad | rs9360921 |
| Varsome | rs9360921 |
| LitVar | rs9360921 |
| Map | rs9360921 |
| PheGenI | rs9360921 |
| Biobank | rs9360921 |
| 1000 genomes | rs9360921 |
| hgdp | rs9360921 |
| ensembl | rs9360921 |
| geneview | rs9360921 |
| scholar | rs9360921 |
| rs9360921 | |
| pharmgkb | rs9360921 |
| gwascentral | rs9360921 |
| openSNP | rs9360921 |
| 23andMe | rs9360921 |
| SNPshot | rs9360921 |
| SNPdbe | rs9360921 |
| MSV3d | rs9360921 |
| GWAS Ctlg | rs9360921 |
| GMAF | 0.09366 |
| Max Magnitude | 0 |
| ? | (G;G) (G;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 20881960 ]
|
| Trait | |
| Title | Hundreds of variants clustered in genomic loci and biological pathways affect human height. |
| Risk Allele | T |
| P-val | 3E-13 |
| Odds Ratio | 0.0400 [NR] meters decrease |
