CFH, complement factor H, 3075

N. diseases: 393; N. variants: 150
Disease: Neurologic Symptoms ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs515299
rs515299
Entrez Id: 3075
Gene Symbol: CFH
CFH
CUI: C0235031
Disease:
Neurologic Symptoms 		0.010 GeneticVariation BEFREE In addition, a heterozygous mutation (causing an S890I change) in factor H of complement was found in the patient who developed chronic renal failure but not in her sister, who presented with exclusive neurologic symptoms. 15800115 2005