rs11574944, ITGAL

N. diseases: 1
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 1.000 0.200 16 30498669 intron variant C/T snv 0.25 0.010 1.000 1 2014 2014