Gene: BNC2 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 54796
Gene Symbol: BNC2
BNC2 		0.600 GermlineCausalMutation disease ORPHANET Rare Variants in BNC2 Are Implicated in Autosomal-Dominant Congenital Lower Urinary-Tract Obstruction. 31051115 2019
Entrez Id: 54796
Gene Symbol: BNC2
BNC2 		0.600 Biomarker disease GENOMICS_ENGLAND Rare Variants in BNC2 Are Implicated in Autosomal-Dominant Congenital Lower Urinary-Tract Obstruction. 31051115 2019
Entrez Id: 54796
Gene Symbol: BNC2
BNC2 		0.600 Biomarker disease HPO