rs387906523, 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 0.882 0.160 18 31593025 missense variant G/A;C snv 0.800 1.000 22 1986 2014
Amyloidosis
CUI: C0002726
Disease: Amyloidosis
93 0.882 0.160 18 31593025 missense variant G/A;C snv 0.010 1.000 1 2018 2018
Cerebral Amyloid Angiopathy
CUI: C0085220
Disease: Cerebral Amyloid Angiopathy
22 0.882 0.160 18 31593025 missense variant G/A;C snv 0.010 1.000 1 2018 2018