Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 22995
Gene Symbol: CEP152
CEP152 		0.700 GeneticVariation disease UNIPROT Mutations in centrosomal protein CEP152 in primary microcephaly families linked to MCPH4. 20598275 2010
Entrez Id: 22995
Gene Symbol: CEP152
CEP152 		0.700 CausalMutation disease CLINVAR
Entrez Id: 22995
Gene Symbol: CEP152
CEP152 		0.700 Biomarker disease CTD_human
Entrez Id: 22995
Gene Symbol: CEP152
CEP152 		0.700 GeneticVariation disease CLINVAR
Entrez Id: 22995
Gene Symbol: CEP152
CEP152 		0.700 Biomarker disease GENOMICS_ENGLAND