rs267607110, TGFBI

N. diseases: 4
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Lattice corneal dystrophy Type I
CUI: C1690006
Disease: Lattice corneal dystrophy Type I
13 0.851 0.160 5 136056769 missense variant C/A snv 0.720 0.909 11 1998 2014
Amyloid of cornea
CUI: C2939149
Disease: Amyloid of cornea
5 0.851 0.160 5 136056769 missense variant C/A snv 0.010 1 2004 2004
Corneal dystrophy, Lattice type 3
CUI: C0339273
Disease: Corneal dystrophy, Lattice type 3
14 0.851 0.160 5 136056769 missense variant C/A snv 0.010 1 2004 2004
Familial Amyloid Polyneuropathy, Type V
CUI: C0155127
Disease: Familial Amyloid Polyneuropathy, Type V
19 0.851 0.160 5 136056769 missense variant C/A snv 0.010 1.000 1 2004 2004