Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 4171
Gene Symbol: MCM2
MCM2 		0.700 GeneticVariation disease UNIPROT Whole Exome Sequencing Identified MCM2 as a Novel Causative Gene for Autosomal Dominant Nonsyndromic Deafness in a Chinese Family. 26196677 2015
Entrez Id: 4171
Gene Symbol: MCM2
MCM2 		0.700 Biomarker disease CLINGEN Whole Exome Sequencing Identified MCM2 as a Novel Causative Gene for Autosomal Dominant Nonsyndromic Deafness in a Chinese Family. 26196677 2015
Entrez Id: 4171
Gene Symbol: MCM2
MCM2 		0.700 Biomarker disease CTD_human
Entrez Id: 4171
Gene Symbol: MCM2
MCM2 		0.700 CausalMutation disease CLINVAR