rs2489188, TGFBR3

N. diseases: 2
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 0.925 0.200 1 91866932 intron variant C/T snv 0.65 0.010 1.000 1 2012 2012
Uveitis
CUI: C0042164
Disease: Uveitis
43 0.925 0.200 1 91866932 intron variant C/T snv 0.65 0.010 1.000 1 2012 2012