CFH, complement factor H, 3075

N. diseases: 393; N. variants: 150
Disease: HEMOLYTIC UREMIC SYNDROME, ATYPICAL, SUSCEPTIBILITY TO, 1 ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs121913059
rs121913059
Entrez Id: 3075
Gene Symbol: CFH
CFH
CUI: C2749604
Disease:
HEMOLYTIC UREMIC SYNDROME, ATYPICAL, SUSCEPTIBILITY TO, 1 		T 0.700 SusceptibilityMutation CLINVAR