Source: ALL

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 718
Gene Symbol: C3
C3
CUI: C0017921
Disease: Glycogen storage disease type II
Glycogen storage disease type II 		0.030 GeneticVariation BEFREE In this study, we investigated the associations of haplotype-tagging single nucleotide polymorphisms (SNPs) in the complement component 3 (C3) gene with both neovascular AMD and PCV, and potential epistatic effects on C3. 25388911

2014
Entrez Id: 718
Gene Symbol: C3
C3
CUI: C0017921
Disease: Glycogen storage disease type II
Glycogen storage disease type II 		0.030 GeneticVariation BEFREE To investigate whether the previously reported noncoding variant of the complement factor H (CFH) gene and two coding variants of the complement component 3 (C3) gene are associated with exudative age-related macular degeneration (AMD) in Chinese patients. 19850835

2010
Entrez Id: 718
Gene Symbol: C3
C3
CUI: C0017921
Disease: Glycogen storage disease type II
Glycogen storage disease type II 		0.030 Biomarker BEFREE Complement component 3: an assessment of association with AMD and analysis of gene-gene and gene-environment interactions in a Northern Irish cohort. 20157618

2010