rs121918086, TTR

N. diseases: 3
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
CUI: C2751492
Disease: AMYLOIDOSIS, HEREDITARY, TRANSTHYRETIN-RELATED
68 1.000 0.120 18 31595160 missense variant G/A snv 0.800 1.000 22 1986 2014
Amyloid Neuropathies, Familial
CUI: C0206245
Disease: Amyloid Neuropathies, Familial
16 1.000 0.120 18 31595160 missense variant G/A snv 0.010 1.000 1 2017 2017
Cardiomyopathies
CUI: C0878544
Disease: Cardiomyopathies
294 1.000 0.120 18 31595160 missense variant G/A snv 0.010 1.000 1 2009 2009