rs104894665, TTR

N. diseases: 5
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 0.851 0.120 18 31593017 missense variant T/C snv 0.800 1.000 22 1986 2014
AMYLOIDOSIS, LEPTOMENINGEAL, TRANSTHYRETIN-RELATED
CUI: C3151470
Disease: AMYLOIDOSIS, LEPTOMENINGEAL, TRANSTHYRETIN-RELATED
5 0.851 0.120 18 31593017 missense variant T/C snv 0.700 0
Amyloidosis
CUI: C0002726
Disease: Amyloidosis
93 0.851 0.120 18 31593017 missense variant T/C snv 0.010 1.000 1 1999 1999
Gastrointestinal amyloidosis
CUI: C0519002
Disease: Gastrointestinal amyloidosis
1 0.851 0.120 18 31593017 missense variant T/C snv 0.010 1.000 1 2007 2007
Gastrointestinal symptom
CUI: C0426576
Disease: Gastrointestinal symptom
7 0.851 0.120 18 31593017 missense variant T/C snv 0.010 1.000 1 2007 2007