rs756465037, LTF

N. diseases: 6
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Keratitis, Herpetic
CUI: C0019357
Disease: Keratitis, Herpetic
0.010 GeneticVariation BEFREE Lactoferrin Glu561Asp polymorphism is associated with the susceptibility to HSV keratitis with a protective role for lactoferrin variants comprising Asp561. 18022620 2008
Reactive systemic amyloidosis
CUI: C0221014
Disease: Reactive systemic amyloidosis
0.010 GeneticVariation BEFREE Lactoferrin Glu561Asp facilitates secondary amyloidosis in the cornea. 15923502 2005
Amyloid of cornea
CUI: C2939149
Disease: Amyloid of cornea
0.010 GeneticVariation BEFREE Lactoferrin Glu561Asp is a key polymorphism related to facilitating amyloid formation in corneal amyloidosis with trichiasis. 15923502 2005
AA amyloidosis
CUI: C3536715
Disease: AA amyloidosis
0.010 GeneticVariation BEFREE Lactoferrin Glu561Asp facilitates secondary amyloidosis in the cornea. 15923502 2005
Trichiasis
CUI: C0221259
Disease: Trichiasis
0.010 GeneticVariation BEFREE Lactoferrin Glu561Asp is a key polymorphism related to facilitating amyloid formation in corneal amyloidosis with trichiasis. 15923502 2005
Corneal dystrophy, Lattice type 3
CUI: C0339273
Disease: Corneal dystrophy, Lattice type 3
0.010 GeneticVariation BEFREE Lactoferrin Glu561Asp is a key polymorphism related to facilitating amyloid formation in corneal amyloidosis with trichiasis. 15923502 2005