{{Rsnum
|rsid=10498760
|Gene=RUNX2
|Chromosome=6
|position=45396059
|Orientation=plus
|GMAF=0.0629
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
|Gene_s=RUNX2
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;C)
| geno3=(C;C)
| CEU | 0.0 | 21.2 | 78.8
| HCB | 0.7 | 13.1 | 86.1
| JPT | 0.0 | 17.7 | 82.3
| YRI | 0.0 | 0.0 | 100.0
| ASW | 0.0 | 3.5 | 96.5
| CHB | 0.7 | 13.1 | 86.1
| CHD | 0.0 | 8.3 | 91.7
| GIH | 1.0 | 32.7 | 66.3
| LWK | 0.0 | 0.9 | 99.1
| MEX | 0.0 | 12.1 | 87.9
| MKK | 0.0 | 0.0 | 0.0
| TSI | 0.0 | 13.7 | 86.3
| HapMapRevision=28
}}

{{Report GE
|PubMed=17878995
|Source=
|AffyProbeset=SNP_A-4211612
|AffyOrientation=reverse
|AlleleA=G
|AlleleB=T
|onGW5=
|rsid=10498760
|ancestral=A
|RiskPopulation=Spain
|RiskAllele=C
|CaseFreq=
|ControlFreq=
|OddsRatioHet=
|OddsRatioHom=
|OddsRatioAll=-
|Disease=Bone mineral density, lower
|DiseaseSymbol=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 Auto
|PMID=17903294
|Title=Genome-wide association and linkage analyses of hemostatic factors and hematological phenotypes in the Framingham Heart Study.
|OA=1
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | Affy500k}}
{{on chip | HumanOmni1Quad}}