Gene: RNF13 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 11342
Gene Symbol: RNF13
RNF13 		0.400 Biomarker disease GENOMICS_ENGLAND Heterozygous RNF13 Gain-of-Function Variants Are Associated with Congenital Microcephaly, Epileptic Encephalopathy, Blindness, and Failure to Thrive. 30595371 2019
Entrez Id: 11342
Gene Symbol: RNF13
RNF13 		0.400 Biomarker disease HPO