rs121918071, TTR

N. diseases: 4
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 0.240 18 31595209 missense variant C/A snv 0.800 1.000 29 1986 2015
Erectile dysfunction
CUI: C0242350
Disease: Erectile dysfunction
44 0.882 0.240 18 31595209 missense variant C/A snv 0.010 1.000 1 2019 2019
Glaucoma
CUI: C0017601
Disease: Glaucoma
198 0.882 0.240 18 31595209 missense variant C/A snv 0.010 1.000 1 2019 2019
Visual symptoms
CUI: C0422943
Disease: Visual symptoms
5 0.882 0.240 18 31595209 missense variant C/A snv 0.010 1.000 1 2019 2019