rs267607161, TTR

N. diseases: 16
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
68 0.742 0.360 18 31598580 missense variant G/T snv 4.0E-06 7.0E-06 0.870 1.000 38 1986 2020
Adenomatous Polyposis Coli
CUI: C0032580
Disease: Adenomatous Polyposis Coli
237 0.742 0.360 18 31598580 missense variant G/T snv 4.0E-06 7.0E-06 0.050 1.000 5 1999 2019
Amyloid Neuropathies, Familial
CUI: C0206245
Disease: Amyloid Neuropathies, Familial
16 0.742 0.360 18 31598580 missense variant G/T snv 4.0E-06 7.0E-06 0.040 1.000 4 2017 2019
Neuropathy
CUI: C0442874
Disease: Neuropathy
110 0.742 0.360 18 31598580 missense variant G/T snv 4.0E-06 7.0E-06 0.030 1.000 3 2010 2019
Amyloidosis
CUI: C0002726
Disease: Amyloidosis
93 0.742 0.360 18 31598580 missense variant G/T snv 4.0E-06 7.0E-06 0.020 1.000 2 2017 2018
Polyneuropathy
CUI: C0152025
Disease: Polyneuropathy
32 0.742 0.360 18 31598580 missense variant G/T snv 4.0E-06 7.0E-06 0.020 1.000 2 2018 2020
Senile cardiac amyloidosis
CUI: C0268407
Disease: Senile cardiac amyloidosis
19 0.742 0.360 18 31598580 missense variant G/T snv 4.0E-06 7.0E-06 0.020 1.000 2 2018 2020
Amyloid Neuropathies
CUI: C0206247
Disease: Amyloid Neuropathies
3 0.742 0.360 18 31598580 missense variant G/T snv 4.0E-06 7.0E-06 0.010 1.000 1 2010 2010
Autonomic neuropathy
CUI: C0259749
Disease: Autonomic neuropathy
7 0.742 0.360 18 31598580 missense variant G/T snv 4.0E-06 7.0E-06 0.010 1.000 1 2018 2018
Cardiomyopathies
CUI: C0878544
Disease: Cardiomyopathies
294 0.742 0.360 18 31598580 missense variant G/T snv 4.0E-06 7.0E-06 0.010 1.000 1 2020 2020
Dry cough
CUI: C0850149
Disease: Dry cough
1 0.742 0.360 18 31598580 missense variant G/T snv 4.0E-06 7.0E-06 0.010 1.000 1 2019 2019
Erectile dysfunction
CUI: C0242350
Disease: Erectile dysfunction
44 0.742 0.360 18 31598580 missense variant G/T snv 4.0E-06 7.0E-06 0.010 1.000 1 2019 2019
Fabry Disease
CUI: C0002986
Disease: Fabry Disease
206 0.742 0.360 18 31598580 missense variant G/T snv 4.0E-06 7.0E-06 0.010 1.000 1 2017 2017
Glaucoma
CUI: C0017601
Disease: Glaucoma
198 0.742 0.360 18 31598580 missense variant G/T snv 4.0E-06 7.0E-06 0.010 1.000 1 2019 2019
Peripheral motor neuropathy
CUI: C0235025
Disease: Peripheral motor neuropathy
20 0.742 0.360 18 31598580 missense variant G/T snv 4.0E-06 7.0E-06 0.010 1.000 1 2018 2018
Visual symptoms
CUI: C0422943
Disease: Visual symptoms
5 0.742 0.360 18 31598580 missense variant G/T snv 4.0E-06 7.0E-06 0.010 1.000 1 2019 2019