rs3118905
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs3118905(A;A) |
| Make rs3118905(A;G) |
| Make rs3118905(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 13 |
| Position | 50531198 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs3118905 |
| dbSNP (classic) | rs3118905 |
| ClinGen | rs3118905 |
| ebi | rs3118905 |
| HLI | rs3118905 |
| Exac | rs3118905 |
| Gnomad | rs3118905 |
| Varsome | rs3118905 |
| LitVar | rs3118905 |
| Map | rs3118905 |
| PheGenI | rs3118905 |
| Biobank | rs3118905 |
| 1000 genomes | rs3118905 |
| hgdp | rs3118905 |
| ensembl | rs3118905 |
| geneview | rs3118905 |
| scholar | rs3118905 |
| rs3118905 | |
| pharmgkb | rs3118905 |
| gwascentral | rs3118905 |
| openSNP | rs3118905 |
| 23andMe | rs3118905 |
| SNPshot | rs3118905 |
| SNPdbe | rs3118905 |
| MSV3d | rs3118905 |
| GWAS Ctlg | rs3118905 |
| GMAF | 0.1556 |
| Max Magnitude | 0 |
| ? | (A;A) (A;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 | A |
| P-val | 1E-45 |
| Odds Ratio | .06 [NR] unit decrease |
[PMID 19570815] A genome-wide association study of northwestern Europeans involves the C-type natriuretic peptide signaling pathway in the etiology of human height variation.
