rs4670779
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs4670779(C;C) |
| Make rs4670779(C;T) |
| Make rs4670779(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 2 |
| Position | 37817201 |
| Gene | LOC344382 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs4670779 |
| dbSNP (classic) | rs4670779 |
| ClinGen | rs4670779 |
| ebi | rs4670779 |
| HLI | rs4670779 |
| Exac | rs4670779 |
| Gnomad | rs4670779 |
| Varsome | rs4670779 |
| LitVar | rs4670779 |
| Map | rs4670779 |
| PheGenI | rs4670779 |
| Biobank | rs4670779 |
| 1000 genomes | rs4670779 |
| hgdp | rs4670779 |
| ensembl | rs4670779 |
| geneview | rs4670779 |
| scholar | rs4670779 |
| rs4670779 | |
| pharmgkb | rs4670779 |
| gwascentral | rs4670779 |
| openSNP | rs4670779 |
| 23andMe | rs4670779 |
| SNPshot | rs4670779 |
| SNPdbe | rs4670779 |
| MSV3d | rs4670779 |
| GWAS Ctlg | rs4670779 |
| GMAF | 0.2167 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 19079262] |
| Trait | Bone mineral density (spine) |
| Title | New sequence variants associated with bone mineral density |
| Risk Allele | T |
| P-val | 0.000004 |
| Odds Ratio | 0.07 [0.04-0.10] SD decrease |
