rs121918077, 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
68 0.882 0.120 18 31592992 missense variant G/C snv 0.800 1.000 22 1986 2014
Amyloidosis
CUI: C0002726
Disease: Amyloidosis
93 0.882 0.120 18 31592992 missense variant G/C snv 0.030 1.000 3 1999 2018
Familial (FPAH)
CUI: C1611743
Disease: Familial (FPAH)
276 0.882 0.120 18 31592992 missense variant G/C snv 0.010 1.000 1 2018 2018