RUNX2, RUNX family transcription factor 2, 860

N. diseases: 405; N. variants: 37
Disease: Cleidocranial Dysplasia ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs730880313
rs730880313
Entrez Id: 860
Gene Symbol: RUNX2
RUNX2
CUI: C0008928
Disease:
Cleidocranial Dysplasia 		ACAGCAGCAGCAGCAGCAGCAACAGCAGCCG 0.700 CausalMutation CLINVAR