rs8181166
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs8181166(C;C) |
| Make rs8181166(C;G) |
| Make rs8181166(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 9 |
| Position | 86501713 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs8181166 |
| dbSNP (classic) | rs8181166 |
| ClinGen | rs8181166 |
| ebi | rs8181166 |
| HLI | rs8181166 |
| Exac | rs8181166 |
| Gnomad | rs8181166 |
| Varsome | rs8181166 |
| LitVar | rs8181166 |
| Map | rs8181166 |
| PheGenI | rs8181166 |
| Biobank | rs8181166 |
| 1000 genomes | rs8181166 |
| hgdp | rs8181166 |
| ensembl | rs8181166 |
| geneview | rs8181166 |
| scholar | rs8181166 |
| rs8181166 | |
| pharmgkb | rs8181166 |
| gwascentral | rs8181166 |
| openSNP | rs8181166 |
| 23andMe | rs8181166 |
| SNPshot | rs8181166 |
| SNPdbe | rs8181166 |
| MSV3d | rs8181166 |
| GWAS Ctlg | rs8181166 |
| GMAF | 0.3646 |
| Max Magnitude | 0 |
| ? | (C;C) (C;G) (G;G) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 20881960 ]
|
| Trait | Height |
| Title | Hundreds of variants clustered in genomic loci and biological pathways affect human height. |
| Risk Allele | C |
| P-val | 3E-12 |
| Odds Ratio | .03 [NR] unit increase |
