rs11118346
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs11118346(C;C) |
| Make rs11118346(C;T) |
| Make rs11118346(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 1 |
| Position | 219570377 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs11118346 |
| dbSNP (classic) | rs11118346 |
| ClinGen | rs11118346 |
| ebi | rs11118346 |
| HLI | rs11118346 |
| Exac | rs11118346 |
| Gnomad | rs11118346 |
| Varsome | rs11118346 |
| LitVar | rs11118346 |
| Map | rs11118346 |
| PheGenI | rs11118346 |
| Biobank | rs11118346 |
| 1000 genomes | rs11118346 |
| hgdp | rs11118346 |
| ensembl | rs11118346 |
| geneview | rs11118346 |
| scholar | rs11118346 |
| rs11118346 | |
| pharmgkb | rs11118346 |
| gwascentral | rs11118346 |
| openSNP | rs11118346 |
| 23andMe | rs11118346 |
| SNPshot | rs11118346 |
| SNPdbe | rs11118346 |
| MSV3d | rs11118346 |
| GWAS Ctlg | rs11118346 |
| GMAF | 0.4073 |
| 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 | 2E-12 |
| Odds Ratio | .03 [NR] unit decrease |
