rs1805110, TGFBR3

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.
Behcet Syndrome
CUI: C0004943
Disease: Behcet Syndrome
243 0.882 0.200 1 91861488 missense variant G/A snv 0.13 0.13 0.020 1.000 2 2012 2015
Uveitis
CUI: C0042164
Disease: Uveitis
43 0.882 0.200 1 91861488 missense variant G/A snv 0.13 0.13 0.010 1.000 1 2012 2012
Uveitis, Intermediate
CUI: C0042166
Disease: Uveitis, Intermediate
10 0.882 0.200 1 91861488 missense variant G/A snv 0.13 0.13 0.010 1.000 1 2015 2015