rs7460090
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs7460090(C;C) |
| Make rs7460090(C;T) |
| Make rs7460090(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 8 |
| Position | 56281604 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs7460090 |
| dbSNP (classic) | rs7460090 |
| ClinGen | rs7460090 |
| ebi | rs7460090 |
| HLI | rs7460090 |
| Exac | rs7460090 |
| Gnomad | rs7460090 |
| Varsome | rs7460090 |
| LitVar | rs7460090 |
| Map | rs7460090 |
| PheGenI | rs7460090 |
| Biobank | rs7460090 |
| 1000 genomes | rs7460090 |
| hgdp | rs7460090 |
| ensembl | rs7460090 |
| geneview | rs7460090 |
| scholar | rs7460090 |
| rs7460090 | |
| pharmgkb | rs7460090 |
| gwascentral | rs7460090 |
| openSNP | rs7460090 |
| 23andMe | rs7460090 |
| SNPshot | rs7460090 |
| SNPdbe | rs7460090 |
| MSV3d | rs7460090 |
| GWAS Ctlg | rs7460090 |
| GMAF | 0.1221 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 20881960 ]
|
| Trait | Height |
| Title | Hundreds of variants clustered in genomic loci and biological pathways affect human height. |
| Risk Allele | T |
| P-val | 8E-27 |
| Odds Ratio | .06 [NR] unit increase |
[PMID 20027299] Transferability and fine-mapping of genome-wide associated loci for adult height across human populations.
