rs9967417
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs9967417(C;C) |
| Make rs9967417(C;G) |
| Make rs9967417(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 18 |
| Position | 49433130 |
| Gene | DYM |
| is a | snp |
| is | mentioned by |
| dbSNP | rs9967417 |
| dbSNP (classic) | rs9967417 |
| ClinGen | rs9967417 |
| ebi | rs9967417 |
| HLI | rs9967417 |
| Exac | rs9967417 |
| Gnomad | rs9967417 |
| Varsome | rs9967417 |
| LitVar | rs9967417 |
| Map | rs9967417 |
| PheGenI | rs9967417 |
| Biobank | rs9967417 |
| 1000 genomes | rs9967417 |
| hgdp | rs9967417 |
| ensembl | rs9967417 |
| geneview | rs9967417 |
| scholar | rs9967417 |
| rs9967417 | |
| pharmgkb | rs9967417 |
| gwascentral | rs9967417 |
| openSNP | rs9967417 |
| 23andMe | rs9967417 |
| SNPshot | rs9967417 |
| SNPdbe | rs9967417 |
| MSV3d | rs9967417 |
| GWAS Ctlg | rs9967417 |
| GMAF | 0.2218 |
| 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 | 9E-25 |
| Odds Ratio | .04 [NR] unit decrease |
| GWAS snp | |
|---|---|
| PMID | [PMID 23563607]
|
| Trait | Height |
| Title | Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture. |
| Risk Allele | G |
| P-val | 5E-9 |
| Odds Ratio | 1.13 [NR] |
