Gene: RUNX2 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 860
Gene Symbol: RUNX2
RUNX2 		0.320 GeneticVariation disease BEFREE Metaphyseal dysplasia with maxillary hypoplasia and brachydactyly in a Finnish woman: first confirmation of a duplication in RUNX2 as pathogenic variant. 25311905 2015
Entrez Id: 860
Gene Symbol: RUNX2
RUNX2 		0.320 GeneticVariation disease BEFREE Metaphyseal dysplasia with maxillary hypoplasia and brachydactyly is caused by a duplication in RUNX2. 23290074 2013
Entrez Id: 860
Gene Symbol: RUNX2
RUNX2 		0.320 Biomarker disease CTD_human