rs5910578
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs5910578(C;C) |
| Make rs5910578(C;T) |
| Make rs5910578(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | X |
| Position | 119433739 |
| Gene | SLC25A43 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs5910578 |
| dbSNP (classic) | rs5910578 |
| ClinGen | rs5910578 |
| ebi | rs5910578 |
| HLI | rs5910578 |
| Exac | rs5910578 |
| Gnomad | rs5910578 |
| Varsome | rs5910578 |
| LitVar | rs5910578 |
| Map | rs5910578 |
| PheGenI | rs5910578 |
| Biobank | rs5910578 |
| 1000 genomes | rs5910578 |
| hgdp | rs5910578 |
| ensembl | rs5910578 |
| geneview | rs5910578 |
| scholar | rs5910578 |
| rs5910578 | |
| pharmgkb | rs5910578 |
| gwascentral | rs5910578 |
| openSNP | rs5910578 |
| 23andMe | rs5910578 |
| SNPshot | rs5910578 |
| SNPdbe | rs5910578 |
| MSV3d | rs5910578 |
| GWAS Ctlg | rs5910578 |
| GMAF | 0.266 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 21623375] |
| Trait | |
| Title | Genome-wide association identifies three new susceptibility loci for Paget's disease of bone. |
| Risk Allele | C |
| P-val | 1E-7 |
| Odds Ratio | 1.3400 [NR] |
