rs2957128
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs2957128(A;A) |
| Make rs2957128(A;G) |
| Make rs2957128(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 18 |
| Position | 62393502 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs2957128 |
| dbSNP (classic) | rs2957128 |
| ClinGen | rs2957128 |
| ebi | rs2957128 |
| HLI | rs2957128 |
| Exac | rs2957128 |
| Gnomad | rs2957128 |
| Varsome | rs2957128 |
| LitVar | rs2957128 |
| Map | rs2957128 |
| PheGenI | rs2957128 |
| Biobank | rs2957128 |
| 1000 genomes | rs2957128 |
| hgdp | rs2957128 |
| ensembl | rs2957128 |
| geneview | rs2957128 |
| scholar | rs2957128 |
| rs2957128 | |
| pharmgkb | rs2957128 |
| gwascentral | rs2957128 |
| openSNP | rs2957128 |
| 23andMe | rs2957128 |
| SNPshot | rs2957128 |
| SNPdbe | rs2957128 |
| MSV3d | rs2957128 |
| GWAS Ctlg | rs2957128 |
| GMAF | 0.4848 |
| 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 | A |
| P-val | 2E-11 |
| Odds Ratio | 1.46 [1.30-1.63] |
