rs76992529, TTR

N. diseases: 36
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.
Pain
CUI: C0030193
Disease: Pain
196 0.653 0.560 18 31598655 missense variant G/A snv 1.1E-03 4.9E-03 0.010 1.000 1 2016 2016
Pancytopenia
CUI: C0030312
Disease: Pancytopenia
15 0.653 0.560 18 31598655 missense variant G/A snv 1.1E-03 4.9E-03 0.700 0
Peripheral Nervous System Diseases
CUI: C4721453
Disease: Peripheral Nervous System Diseases
69 0.653 0.560 18 31598655 missense variant G/A snv 1.1E-03 4.9E-03 0.020 1.000 2 2012 2015
Peripheral Neuropathy
CUI: C0031117
Disease: Peripheral Neuropathy
81 0.653 0.560 18 31598655 missense variant G/A snv 1.1E-03 4.9E-03 0.020 1.000 2 2012 2015
Pneumonia
CUI: C0032285
Disease: Pneumonia
33 0.653 0.560 18 31598655 missense variant G/A snv 1.1E-03 4.9E-03 0.700 0
Primary amyloidosis
CUI: C0268381
Disease: Primary amyloidosis
11 0.653 0.560 18 31598655 missense variant G/A snv 1.1E-03 4.9E-03 0.010 1.000 1 2009 2009
Reactive systemic amyloidosis
CUI: C0221014
Disease: Reactive systemic amyloidosis
11 0.653 0.560 18 31598655 missense variant G/A snv 1.1E-03 4.9E-03 0.010 1.000 1 2011 2011
Senile cardiac amyloidosis
CUI: C0268407
Disease: Senile cardiac amyloidosis
19 0.653 0.560 18 31598655 missense variant G/A snv 1.1E-03 4.9E-03 0.100 1.000 14 1997 2019
Sessile Serrated Adenoma/Polyp
CUI: C2732618
Disease: Sessile Serrated Adenoma/Polyp
6 0.653 0.560 18 31598655 missense variant G/A snv 1.1E-03 4.9E-03 0.010 1.000 1 1990 1990
Transthyretin cardiac amyloidosis
CUI: C4531196
Disease: Transthyretin cardiac amyloidosis
2 0.653 0.560 18 31598655 missense variant G/A snv 1.1E-03 4.9E-03 0.040 1.000 4 2012 2017
Transthyretin related familial amyloid cardiomyopathy
CUI: C4275067
Disease: Transthyretin related familial amyloid cardiomyopathy
1 0.653 0.560 18 31598655 missense variant G/A snv 1.1E-03 4.9E-03 0.700 0