rs936551, CPLX1

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 4 827702 upstream gene variant A/G snv 0.52 0.700 1.000 1 2013 2013