CFP, complement factor properdin, 5199

N. diseases: 108; N. variants: 7
Disease: Properdin Deficiency, Type III ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs132630261
rs132630261
Entrez Id: 5199
Gene Symbol: CFP
CFP
CUI: C1839456
Disease:
Properdin Deficiency, Type III 		C 0.700 CausalMutation CLINVAR