C3, complement C3, 718

N. diseases: 343; N. variants: 49
Disease: Glycogen storage disease type II ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1047286
rs1047286
Entrez Id: 718
Gene Symbol: C3
C3
CUI: C0017921
Disease:
Glycogen storage disease type II 		0.010 GeneticVariation BEFREE In contrast, the C3 variants rs2230199 and rs1047286 were not associated with exudative AMD in the studied subjects. 19850835 2010