CFH, complement factor H, 3075

N. diseases: 393; N. variants: 150
Disease: Impaired cognition ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1061170
rs1061170
Entrez Id: 3075
Gene Symbol: CFH
CFH
CUI: C0338656
Disease:
Impaired cognition 		0.010 GeneticVariation BEFREE The C3F and Y402H polymorphisms are strong independent predictors of moderate-to-severe neurocognitive dysfunction at 1 day following CEA. 20841369 2011