Gene: SDCCAG8 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 10806
Gene Symbol: SDCCAG8
SDCCAG8 		0.110 GeneticVariation disease BEFREE A mutation in SDCCAG8 is also associated with Bardet-Biedl syndrome (BBS), characterized by NPHP, obesity, polydactyly, and rod-cone dystrophy. 31534065 2019
Entrez Id: 10806
Gene Symbol: SDCCAG8
SDCCAG8 		0.110 Biomarker disease HPO