rs121918068, TTR

N. diseases: 6
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 0.882 0.200 18 31592983 missense variant T/A;C snv 0.810 1.000 23 1986 2017
Amyloidosis
CUI: C0002726
Disease: Amyloidosis
93 0.882 0.200 18 31592983 missense variant T/A;C snv 0.020 1.000 2 2007 2017
Adenomatous Polyposis Coli
CUI: C0032580
Disease: Adenomatous Polyposis Coli
237 0.882 0.200 18 31592983 missense variant T/A;C snv 0.010 1.000 1 2017 2017
Amyloid Neuropathies, Familial
CUI: C0206245
Disease: Amyloid Neuropathies, Familial
16 0.882 0.200 18 31592983 missense variant T/A;C snv 0.010 1.000 1 2007 2007
Peripheral Nervous System Diseases
CUI: C4721453
Disease: Peripheral Nervous System Diseases
69 0.882 0.200 18 31592983 missense variant T/A;C snv 0.010 1.000 1 2007 2007
Peripheral Neuropathy
CUI: C0031117
Disease: Peripheral Neuropathy
81 0.882 0.200 18 31592983 missense variant T/A;C snv 0.010 1.000 1 2007 2007