rs10494112
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs10494112(A;A) |
| Make rs10494112(A;G) |
| Make rs10494112(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 1 |
| Position | 109809855 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs10494112 |
| dbSNP (classic) | rs10494112 |
| ClinGen | rs10494112 |
| ebi | rs10494112 |
| HLI | rs10494112 |
| Exac | rs10494112 |
| Gnomad | rs10494112 |
| Varsome | rs10494112 |
| LitVar | rs10494112 |
| Map | rs10494112 |
| PheGenI | rs10494112 |
| Biobank | rs10494112 |
| 1000 genomes | rs10494112 |
| hgdp | rs10494112 |
| ensembl | rs10494112 |
| geneview | rs10494112 |
| scholar | rs10494112 |
| rs10494112 | |
| pharmgkb | rs10494112 |
| gwascentral | rs10494112 |
| openSNP | rs10494112 |
| 23andMe | rs10494112 |
| SNPshot | rs10494112 |
| SNPdbe | rs10494112 |
| MSV3d | rs10494112 |
| GWAS Ctlg | rs10494112 |
| GMAF | 0.1244 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
related to Paget’s disease of bone 23andMe blog.
| GWAS snp | |
|---|---|
| PMID | [PMID 21623375] |
| Trait | |
| Title | Genome-wide association identifies three new susceptibility loci for Paget's disease of bone. |
| Risk Allele | G |
| P-val | 7E-35 |
| Odds Ratio | 1.7200 [1.57-1.87] |
