rs484959
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs484959(A;A) |
| Make rs484959(A;G) |
| Make rs484959(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 1 |
| Position | 109823461 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs484959 |
| dbSNP (classic) | rs484959 |
| ClinGen | rs484959 |
| ebi | rs484959 |
| HLI | rs484959 |
| Exac | rs484959 |
| Gnomad | rs484959 |
| Varsome | rs484959 |
| LitVar | rs484959 |
| Map | rs484959 |
| PheGenI | rs484959 |
| Biobank | rs484959 |
| 1000 genomes | rs484959 |
| hgdp | rs484959 |
| ensembl | rs484959 |
| geneview | rs484959 |
| scholar | rs484959 |
| rs484959 | |
| pharmgkb | rs484959 |
| gwascentral | rs484959 |
| openSNP | rs484959 |
| 23andMe | rs484959 |
| SNPshot | rs484959 |
| SNPdbe | rs484959 |
| MSV3d | rs484959 |
| GWAS Ctlg | rs484959 |
| GMAF | 0.4991 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
related to Paget’s disease of bone 23andMe blog.
| GWAS snp | |
|---|---|
| PMID | [PMID 20436471 ]
|
| Trait | Paget's disease |
| Title | Genome-wide association study identifies variants at CSF1, OPTN and TNFRSF11A as genetic risk factors for Paget's disease of bone |
| Risk Allele | |
| P-val | 5E-24 |
| Odds Ratio | 1.82 [1.61-2.04] |
