Runt-related transcription factor 2 (RUNX2) plays important roles in osteoblast
differentiation, tooth development and chondrocyte maturation; hence its involvement in
craniofacial development is paramount. Mutation in RUNX2 is implicated with cleidocranial
dysplasia; a bone development disorder, while single nucleotide polymorphism (SNP) in RUNX2 is
associated with Class II/2 malocclusion. This study aimed to determine RUNX2 SNP of DNA marker
(rs6930053) in malocclusion patients from local population. (Copied from article).