rs121909715, GSN

N. diseases: 8
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.
Meretoja syndrome
CUI: C1622345
Disease: Meretoja syndrome
1 0.790 0.160 9 121310819 missense variant G/A;T snv 4.0E-06 0.800 1.000 2 1990 1992
Neurodegenerative Disorders
CUI: C0524851
Disease: Neurodegenerative Disorders
85 0.790 0.160 9 121310819 missense variant G/A;T snv 4.0E-06 0.010 1.000 1 2003 2003
Lattice corneal dystrophy Type II
CUI: C1628319
Disease: Lattice corneal dystrophy Type II
4 0.790 0.160 9 121310819 missense variant G/A;T snv 4.0E-06 0.040 1.000 4 1995 2011
Amyloid of cornea
CUI: C2939149
Disease: Amyloid of cornea
5 0.790 0.160 9 121310819 missense variant G/A;T snv 4.0E-06 0.010 1.000 1 2014 2014
Corneal dystrophy, Lattice type 3
CUI: C0339273
Disease: Corneal dystrophy, Lattice type 3
14 0.790 0.160 9 121310819 missense variant G/A;T snv 4.0E-06 0.010 1.000 1 2014 2014
Amyloidosis, Familial
CUI: C0740340
Disease: Amyloidosis, Familial
12 0.790 0.160 9 121310819 missense variant G/A;T snv 4.0E-06 0.050 1.000 5 1991 2017
Amyloidosis
CUI: C0002726
Disease: Amyloidosis
93 0.790 0.160 9 121310819 missense variant G/A;T snv 4.0E-06 0.060 1.000 6 1991 2018
Familial Amyloid Polyneuropathy, Type V
19 0.790 0.160 9 121310819 missense variant G/A;T snv 4.0E-06 0.020 1.000 2 1992 2018