rs121909585, C3

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.
HEMOLYTIC UREMIC SYNDROME, ATYPICAL, SUSCEPTIBILITY TO, 5
8 0.925 0.120 19 6692971 missense variant C/T snv 0.800 1.000 4 2008 2010
Atypical Hemolytic Uremic Syndrome
CUI: C2931788
Disease: Atypical Hemolytic Uremic Syndrome
42 0.925 0.120 19 6692971 missense variant C/T snv 0.010 1.000 1 2019 2019
Hematuria
CUI: C0018965
Disease: Hematuria
31 0.925 0.120 19 6692971 missense variant C/T snv 0.010 1.000 1 2019 2019
Thrombotic Microangiopathies
CUI: C2717961
Disease: Thrombotic Microangiopathies
8 0.925 0.120 19 6692971 missense variant C/T snv 0.010 1.000 1 2019 2019