rs104894664, 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 0.120 18 31592959 missense variant G/A snv 0.700 0
Amyloidosis
CUI: C0002726
Disease: Amyloidosis
93 0.882 0.120 18 31592959 missense variant G/A snv 0.030 1.000 3 2003 2011
Amyloid Neuropathies, Familial
CUI: C0206245
Disease: Amyloid Neuropathies, Familial
16 0.882 0.120 18 31592959 missense variant G/A snv 0.010 1.000 1 2010 2010
Peripheral Nervous System Diseases
CUI: C4721453
Disease: Peripheral Nervous System Diseases
69 0.882 0.120 18 31592959 missense variant G/A snv 0.010 1.000 1 2003 2003
Peripheral Neuropathy
CUI: C0031117
Disease: Peripheral Neuropathy
81 0.882 0.120 18 31592959 missense variant G/A snv 0.010 1.000 1 2003 2003
Polyneuropathy
CUI: C0152025
Disease: Polyneuropathy
32 0.882 0.120 18 31592959 missense variant G/A snv 0.010 1.000 1 2006 2006