rs5743733, TLR7

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 0.280 X 12871589 intron variant C/G;T snv 0.010 1.000 1 2013 2013
Hepatitis C
CUI: C0019196
Disease: Hepatitis C
347 0.925 0.280 X 12871589 intron variant C/G;T snv 0.010 1.000 1 2015 2015