rs121918079, 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
68 0.790 0.280 18 31595143 missense variant T/C snv 0.810 1.000 23 1986 2014
Amyloid Neuropathies, Familial
CUI: C0206245
Disease: Amyloid Neuropathies, Familial
16 0.790 0.280 18 31595143 missense variant T/C snv 0.040 1.000 4 1994 2020
Amyloidosis
CUI: C0002726
Disease: Amyloidosis
93 0.790 0.280 18 31595143 missense variant T/C snv 0.020 1.000 2 2007 2009
Cardiomyopathies
CUI: C0878544
Disease: Cardiomyopathies
294 0.790 0.280 18 31595143 missense variant T/C snv 0.020 1.000 2 2018 2020
Polyneuropathy
CUI: C0152025
Disease: Polyneuropathy
32 0.790 0.280 18 31595143 missense variant T/C snv 0.020 1.000 2 1998 2018
Adenomatous Polyposis Coli
CUI: C0032580
Disease: Adenomatous Polyposis Coli
237 0.790 0.280 18 31595143 missense variant T/C snv 0.010 1.000 1 1999 1999
Autonomic neuropathy
CUI: C0259749
Disease: Autonomic neuropathy
7 0.790 0.280 18 31595143 missense variant T/C snv 0.010 1.000 1 2007 2007
Kidney Diseases
CUI: C0022658
Disease: Kidney Diseases
140 0.790 0.280 18 31595143 missense variant T/C snv 0.010 1.000 1 2007 2007
Renal Insufficiency
CUI: C1565489
Disease: Renal Insufficiency
42 0.790 0.280 18 31595143 missense variant T/C snv 0.010 1.000 1 2017 2017
Senile systemic amyloidosis
CUI: C0342623
Disease: Senile systemic amyloidosis
2 0.790 0.280 18 31595143 missense variant T/C snv 0.010 1.000 1 2018 2018