rs10498760
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs10498760(A;A) |
| Make rs10498760(A;C) |
| Make rs10498760(C;C) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 6 |
| Position | 45396059 |
| Gene | RUNX2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs10498760 |
| dbSNP (classic) | rs10498760 |
| ClinGen | rs10498760 |
| ebi | rs10498760 |
| HLI | rs10498760 |
| Exac | rs10498760 |
| Gnomad | rs10498760 |
| Varsome | rs10498760 |
| LitVar | rs10498760 |
| Map | rs10498760 |
| PheGenI | rs10498760 |
| Biobank | rs10498760 |
| 1000 genomes | rs10498760 |
| hgdp | rs10498760 |
| ensembl | rs10498760 |
| geneview | rs10498760 |
| scholar | rs10498760 |
| rs10498760 | |
| pharmgkb | rs10498760 |
| gwascentral | rs10498760 |
| openSNP | rs10498760 |
| 23andMe | rs10498760 |
| SNPshot | rs10498760 |
| SNPdbe | rs10498760 |
| MSV3d | rs10498760 |
| GWAS Ctlg | rs10498760 |
| GMAF | 0.0629 |
| Max Magnitude | 0 |
| ? | (A;A) (A;C) (C;C) | 28 |
|---|---|---|
|
| ||
| Rs10498760 | |
|---|---|
| PubMed | [PMID 17878995] |
| Affy Probeset | SNP_A-4211612 |
| Affy Orientation | reverse |
| On GW 5.0 | |
| Alleles A/B | G/T |
| Ancestral | A |
| Population | Spain |
| Allele | C |
| Case Freq. | |
| Control Freq. | |
| Odds Ratio Het | |
| Odds Ratio Hom | |
| Odds Ratio All | - |
| Disease | Bone mineral density, lower (BMD-L) |
rs10498760 is in linkage disequilibrium with a polymorphism that increases susceptibility to Bone mineral density variations, lower for carriers of the C allele [PMID 17878995]
[PMID 17903294
] Genome-wide association and linkage analyses of hemostatic factors and hematological phenotypes in the Framingham Heart Study.
