rs121918069, 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 0.925 0.200 18 31595152 missense variant T/A;G snv 0.820 1.000 35 1986 2016
Adenomatous Polyposis Coli
CUI: C0032580
Disease: Adenomatous Polyposis Coli
237 0.925 0.200 18 31595152 missense variant T/A;G snv 0.020 1.000 2 2007 2008
Amyloid Neuropathies, Familial
CUI: C0206245
Disease: Amyloid Neuropathies, Familial
16 0.925 0.200 18 31595152 missense variant T/A;G snv 0.010 1.000 1 2007 2007