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.

rs10498760

Parent Gene: RUNX2

Importance: 1
Less common allele: A = 7%
More common allele: C = 93%
My Genotype: Log In