rs759304648, GSN

N. diseases: 9
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 II
CUI: C1628319
Disease: Lattice corneal dystrophy Type II
4 0.790 0.240 9 121312479 synonymous variant G/A snv 8.0E-05 3.5E-05 0.040 1.000 4 1995 2000
Amyloidosis
CUI: C0002726
Disease: Amyloidosis
93 0.790 0.240 9 121312479 synonymous variant G/A snv 8.0E-05 3.5E-05 0.030 1.000 3 2002 2007
Amyloidosis, Familial
CUI: C0740340
Disease: Amyloidosis, Familial
12 0.790 0.240 9 121312479 synonymous variant G/A snv 8.0E-05 3.5E-05 0.020 1.000 2 1997 1999
Blood Coagulation Disorders
CUI: C0005779
Disease: Blood Coagulation Disorders
31 0.790 0.240 9 121312479 synonymous variant G/A snv 8.0E-05 3.5E-05 0.010 1.000 1 2000 2000
Cutis Laxa
CUI: C0010495
Disease: Cutis Laxa
21 0.790 0.240 9 121312479 synonymous variant G/A snv 8.0E-05 3.5E-05 0.010 1.000 1 2009 2009
Hypotension, Orthostatic
CUI: C0020651
Disease: Hypotension, Orthostatic
21 0.790 0.240 9 121312479 synonymous variant G/A snv 8.0E-05 3.5E-05 0.010 1.000 1 2010 2010
Inherited systemic amyloidosis
CUI: C1719316
Disease: Inherited systemic amyloidosis
1 0.790 0.240 9 121312479 synonymous variant G/A snv 8.0E-05 3.5E-05 0.010 1.000 1 1999 1999
Polyneuropathy
CUI: C0152025
Disease: Polyneuropathy
32 0.790 0.240 9 121312479 synonymous variant G/A snv 8.0E-05 3.5E-05 0.010 1.000 1 2009 2009
Sleep Apnea Syndromes
CUI: C0037315
Disease: Sleep Apnea Syndromes
18 0.790 0.240 9 121312479 synonymous variant G/A snv 8.0E-05 3.5E-05 0.010 1.000 1 1999 1999