rs1518111, IL19;IL10

N. diseases: 1
Source: GWASDB ×
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
40 0.790 0.360 1 206771300 intron variant T/C snv 0.71 0.830 1.000 1 2010 2015