rs121918097, TTR

N. diseases: 10
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, HEREDITARY, TRANSTHYRETIN-RELATED
CUI: C2751492
Disease: AMYLOIDOSIS, HEREDITARY, TRANSTHYRETIN-RELATED
68 0.790 0.280 18 31595137 missense variant G/A snv 0.700 1.000 20 1986 2007
AMYLOIDOSIS, LEPTOMENINGEAL, TRANSTHYRETIN-RELATED
CUI: C3151470
Disease: AMYLOIDOSIS, LEPTOMENINGEAL, TRANSTHYRETIN-RELATED
5 0.790 0.280 18 31595137 missense variant G/A snv 0.700 0
Amyloidosis
CUI: C0002726
Disease: Amyloidosis
93 0.790 0.280 18 31595137 missense variant G/A snv 0.010 1.000 1 2006 2006
Cardiomyopathies
CUI: C0878544
Disease: Cardiomyopathies
294 0.790 0.280 18 31595137 missense variant G/A snv 0.010 1.000 1 2005 2005
Dysarthria
CUI: C0013362
Disease: Dysarthria
54 0.790 0.280 18 31595137 missense variant G/A snv 0.010 1.000 1 2016 2016
Dyspnea
CUI: C0013404
Disease: Dyspnea
26 0.790 0.280 18 31595137 missense variant G/A snv 0.010 1.000 1 2005 2005
Hemiparesis
CUI: C0018989
Disease: Hemiparesis
6 0.790 0.280 18 31595137 missense variant G/A snv 0.010 1.000 1 2016 2016
Plaque, Amyloid
CUI: C2936349
Disease: Plaque, Amyloid
10 0.790 0.280 18 31595137 missense variant G/A snv 0.010 1.000 1 2001 2001
Pneumonia, Viral
CUI: C0032310
Disease: Pneumonia, Viral
1 0.790 0.280 18 31595137 missense variant G/A snv 0.010 1.000 1 2006 2006
Subarachnoid Hemorrhage
CUI: C0038525
Disease: Subarachnoid Hemorrhage
26 0.790 0.280 18 31595137 missense variant G/A snv 0.010 1.000 1 2001 2001