rs7864648
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs7864648(G;G) |
| Make rs7864648(G;T) |
| Make rs7864648(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 9 |
| Position | 16368734 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs7864648 |
| dbSNP (classic) | rs7864648 |
| ClinGen | rs7864648 |
| ebi | rs7864648 |
| HLI | rs7864648 |
| Exac | rs7864648 |
| Gnomad | rs7864648 |
| Varsome | rs7864648 |
| LitVar | rs7864648 |
| Map | rs7864648 |
| PheGenI | rs7864648 |
| Biobank | rs7864648 |
| 1000 genomes | rs7864648 |
| hgdp | rs7864648 |
| ensembl | rs7864648 |
| geneview | rs7864648 |
| scholar | rs7864648 |
| rs7864648 | |
| pharmgkb | rs7864648 |
| gwascentral | rs7864648 |
| openSNP | rs7864648 |
| 23andMe | rs7864648 |
| SNPshot | rs7864648 |
| SNPdbe | rs7864648 |
| MSV3d | rs7864648 |
| GWAS Ctlg | rs7864648 |
| GMAF | 0.3026 |
| 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 | 2E-8 |
| Odds Ratio | 0.0200 [NR] meters increase |
