CFH, complement factor H, 3075

N. diseases: 393; N. variants: 150
Disease: Hemolytic-Uremic Syndrome ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs121913060
rs121913060
Entrez Id: 3075
Gene Symbol: CFH
CFH
CUI: C0019061
Disease:
Hemolytic-Uremic Syndrome 		0.010 GeneticVariation BEFREE Hemolytic uremic syndrome: a factor H mutation (E1172Stop) causes defective complement control at the surface of endothelial cells. 17229916 2007