rs1800576, THBD

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, 6
CUI: C2752036
Disease: HEMOLYTIC UREMIC SYNDROME, ATYPICAL, SUSCEPTIBILITY TO, 6
7 0.925 0.080 20 23049378 missense variant C/T snv 2.0E-03 2.5E-03 0.700 1.000 2 2009 2010
Cerebrovascular Disorders
CUI: C0007820
Disease: Cerebrovascular Disorders
56 0.925 0.080 20 23049378 missense variant C/T snv 2.0E-03 2.5E-03 0.010 1.000 1 2000 2000
Myocardial Infarction
CUI: C0027051
Disease: Myocardial Infarction
680 0.925 0.080 20 23049378 missense variant C/T snv 2.0E-03 2.5E-03 0.010 1.000 1 1998 1998
Venous Thromboembolism
CUI: C1861172
Disease: Venous Thromboembolism
408 0.925 0.080 20 23049378 missense variant C/T snv 2.0E-03 2.5E-03 0.010 1 2005 2005