rs920832709, GSN

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.
Amyloidosis
CUI: C0002726
Disease: Amyloidosis
93 0.851 0.200 9 121321384 synonymous variant G/T snv 0.030 1.000 3 2002 2007
Lattice corneal dystrophy Type II
CUI: C1628319
Disease: Lattice corneal dystrophy Type II
4 0.851 0.200 9 121321384 synonymous variant G/T snv 0.020 1.000 2 1995 2000
Primary Systemic Amyloidosis
CUI: C0281479
Disease: Primary Systemic Amyloidosis
10 0.851 0.200 9 121321384 synonymous variant G/T snv 0.010 1.000 1 1997 1997
Systemic amyloidosis
CUI: C0268380
Disease: Systemic amyloidosis
10 0.851 0.200 9 121321384 synonymous variant G/T snv 0.010 1.000 1 1997 1997