RS104893995 RUNX2

Health Risk Chr 6:45431945
Upload your DNA to see your genotype for this variant.
What This Variant Does
"[OMIM:?]
Associated Conditions
Cleidocranial dysostosis
Cleidocranial dysostosis
RUNX2-related disorder
Metaphyseal dysplasia-maxillary hypoplasia-brachydacty syndrome
Cleidocranial dysostosis
Cleidocranial dysostosis
RUNX2-related disorder
Metaphyseal dysplasia-maxillary hypoplasia-brachydacty syndrome
Other Variants in RUNX2
rs730880313 rs104893988 rs606231174 rs104893989 rs104893990 rs1582232661 rs730880314 rs104893991 rs104893992 rs104893993
Ask Dr. Hemsworth about this variant